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SC Reg 60-93

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SC Reg 60-93 Standards for Licensing Facilities for Chemically Dependent or Addicted Persons

Jurisdiction: SC Agency: South Carolina Department of Mental Health (DMH); Department of Public Health; and the behavioral-health licensing boards (LLR)
DETOX (100%) OTP (100%) OUTPATIENT (100%) SUD_IOP (60%) SUD_RESIDENTIAL (100%)
Plain-English summary

This South Carolina regulation establishes comprehensive licensing standards for facilities serving chemically dependent or addicted persons, covering both outpatient and residential substance use disorder treatment settings. Operators must obtain a license from the Department before providing services, comply with staffing, patient records, medication management, physical plant, and quality improvement requirements, and submit to inspections and enforcement actions. The regulation explicitly governs residential SUD treatment programs, withdrawal management programs (both medical and social), opioid treatment programs (including medication units), and outpatient SUD facilities.

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Regulation text
60–93. S TANDARDS FOR LICENSING FACILITIES FOR CHEMICALLY
DEPENDENT OR ADDICTED PERSONS.
(Statutory Authority: S.C. Code §§ 44–7–260 et seq.)
Editor’s Note
Unless otherwise noted, the following constitutes the history for 60–93, 101 to 3223.
HISTORY: Added by State Register Volume 12, Issue No. 2, eff February 26, 1988. Amended by State
Register Volume 25, Issue No. 5, Part 1, eff May 25, 2001; State Register Volume 34, Issue No. 6, eff June
25, 2010; State Register Volume 39, Issue No. 6, Doc. No. 4464, eff June 26, 2015; SCSR 44–6 Doc. No.
4954, eff June 26, 2020. Transferred from 61–93 by SCSR 49–5 Doc. No. 5352, eff May 23, 2025.
The Table of Contents appears as published in SCSR 44-6 Doc. No. 4954; there is no text for ‘‘504. Staffing
for Withdrawal Management Programs (I)’’ or ‘‘2616. Seclusion Room (II)’’.
TABLE OF CONTENTS
 
SECTION 100—DEFINITIONS AND LICENSURE
101. Definitions.
102. License Requirements.
 
SECTION 200—ENFORCEMENT OF REGULATIONS
201. General.
202. Inspections and Investigations.
203. Consultations.
 
SECTION 300—ENFORCEMENT ACTIONS
301. General.
302. Violation Classifications.
 
SECTION 400—POLICIES AND PROCEDURES
 
SECTION 500—STAFF AND TRAINING
501. General (II).
502. Administrator (II).
503. Staffing for Residential Treatment Programs (I).
504. Staffing for Withdrawal Management Programs (I).
505. Staffing for Opioid Treatment Programs (I).
506. In-service Training (II).
507. Health Status (I).
508. Counselors (II).
 
SECTION 600—REPORTING
601. Accidents and Incidents (II).
602. Fire and Disasters (II).
603. Communicable Diseases and Animal Bites (I).
604. Administrator Change.
605. Joint Annual Report.
606. Accounting of Controlled Substances (I).
607. Facility Closure.
608. Zero Census.
 
SECTION 700—PATIENT RECORDS
701. Content (II).
702. Screening (I).
703. Assessments for Residential Treatment Programs (II).
704. Assessment for Withdrawal Management Programs (II).
705. Bio-Psycho-Social Assessment Opioid Treatment Program (II).
706. Individual Plan of Care (II).
707. Individual Plan of Care for Opioid Treatment Program (II).
708. Record Maintenance.
 
SECTION 800—ADMISSION (I)
801. General.
802. Residential Facilities.
803. Opioid Treatment Program.
 
SECTION 900—PATIENT CARE, TREATMENT, AND SERVICES
901. General.
902. Residential Facilities (II).
903. Facilities Providing an Opioid Treatment Program.
904. Substance Use Testing for Opioid Treatment Programs (II).
905. Orientation for Patients Admitted to an Opioid Treatment Program.
906. Transportation.
907. Safety Precautions and Restraints (I).
908. Services for Minors (II).
909. Referral Services.
 
SECTION 1000—PATIENT RIGHTS AND ASSURANCES
1001. Informed Consent (II).
1002. Patient Rights (II).
1003. Discharge and Transfer.
 
SECTION 1100—PATIENT PHYSICAL EXAMINATION (I)
 
SECTION 1200—MEDICATION MANAGEMENT
1201. General (I).
1202. Medication Orders (I).
1203. Administering Medication (I).
1204. Pharmacy Services (I).
1205. Medication Containers (I).
1206. Medication Storage (I).
1207. Disposition of Medications (I).
1208. Opioid Treatment Program Take-home Medication (II).
1209. Opioid Treatment Program Guest-Dosing (II).
1210. Security of Medications (I).
 
SECTION 1300—MEAL SERVICE (II)
1301. General (II).
1302. Food and Food Storage (II).
1303. Meals and Services.
1304. Meal Service Personnel for Residential Facilities (II).
1305. Menus.
 
SECTION 1400—EMERGENCY PROCEDURES AND DISASTER PREPAREDNESS
1401. Disaster Preparedness (II).
1402. Licensed Capacity During an Emergency (II).
1403. Emergency Call Numbers (II).
1404. Continuity of Essential Services (II).
 
SECTION 1500—FIRE PREVENTION
1501. Arrangements for Fire Department Response (I).
1502. Fire response Training (I).
1503. Fire Drills (I).
 
SECTION 1600—MAINTENANCE
1601. General (II).
1602. Preventive Maintenance of Emergency Equipment and Supplies (II).
 
SECTION 1700—INFECTION CONTROL AND ENVIRONMENT
1701. Staff Practices.
1702. Tuberculosis Risk Assessment and Screening (I).
1703. Tuberculosis Screening for Patients (I).
1704. Housekeeping (II).
1705. Infectious Waste (I).
1706. Pets (II).
1707. Clean and Soiled Linen and Clothing (II).
 
SECTION 1800—QUALITY IMPROVEMENT PROGRAM (II)
 
SECTION 1900—DESIGN AND CONSTRUCTION
1901. Codes and Standards.
1902. Local and State Codes and Standards (II).
1903. Submission of Plans and Specifications (II).
1904. Construction Inspections.
 
SECTION 2000—FIRE PROTECTION, PREVENTION, AND LIFE SAFETY (I)
 
SECTION 2100—[RESERVED]
 
SECTION 2200—[RESERVED]
 
SECTION 2300—[RESERVED]
 
SECTION 2400—ELECTRICAL
2401. Receptacles (II).
2402. Ground Fault Protection (I).
2403. Exit Signs (I).
2404. Emergency Electric Service (I).
2405. Emergency Generator Service.
 
SECTION 2500—[RESERVED]
 
SECTION 2600—PHYSICAL PLANT
2601. Facility Accommodations and Floor Area (II).
2602. Design (I).
2603. Furnishings and Equipment (I).
2604. Exits (I).
2605. Water Supply and Hygiene (II).
2606. Temperature Control (I).
2607. Cross-connections (I).
2608. Wastewater Systems (I).
2609. Electric Wiring (I).
2610. Panelboards (II).
2611. Lighting.
2612. Heating, Ventilation, and Air Conditioning (II).
2613. Patient Rooms.
2614. Patient Room Floor Area.
2615. Bathrooms and Restrooms.
2616. Seclusion Room (II).
2617. Patient Care Unit and Station for Medical Withdrawal Management (II).
2618. Doors (II).
2619. Elevators (II).
2620. Screens (II).
2621. Janitor’s Closet.
2622. Storage Areas.
2623. Telephone Service.
2624. Location.
2625. Outdoor Area.
 
SECTION 2700—SEVERABILITY (I)
 
SECTION 2800—GENERAL (I)
SECTION 100. DEFINITIONS AND LICENSURE
101. Definitions.
For the purpose of this regulation, the following definitions shall apply:
A. Abuse. Physical abuse or psychological abuse.
1. Physical Abuse. The act of intentionally inflicting or allowing infliction of physical injury on a
Patient by an act or failure to act. Physical abuse includes, but is not limited to, slapping, hitting,
kicking, biting, choking, pinching, burning, actual or attempted sexual battery, use of medication
outside the standards of reasonable medical practice for the purpose of controlling behavior, and
unreasonable confinement. Physical abuse also includes the use of a restrictive or physically intrusive
procedure to control behavior for the purpose of punishment except that of a therapeutic procedure
prescribed by a licensed physician or other legally authorized healthcare professional. Physical abuse
does not include altercations or acts of assault between Patients.
2. Psychological Abuse. The deliberate use of any oral, written, or gestured language or depiction
that includes disparaging or derogatory terms to a Patient or within the Patient’s hearing distance,
regardless of the Patient’s age, ability to comprehend, or disability, including threats or harassment
or other forms of intimidating behavior causing fear, humiliation, degradation, agitation, confusion,
or other forms of serious emotional distress.
B. Administering Medication. The acts of preparing and giving of a single dose of a medication to
the body of a Patient by injection, ingestion, or any other means in accordance with the orders of a
Physician or other Authorized Healthcare Provider.
C. Administrator. The staff member designated by the Licensee to have the authority and
responsibility to manage the Facility and who is in charge of all functions and activities of the Facility.
D. Adult. A person eighteen (18) years of age or older.
E. Aftercare/Continuing Care. Services provided to Patients after discharge from a Facility that
facilitates the Patient’s integration or reintegration into society. Activities may include self-help groups,
supportive work programs, and staff follow-up contacts and interventions.
F. Annual. A time period that requires an activity to be performed at least every twelve (12)
months.
G. Assessment. A procedure for determining the nature and extent of the problems and needs of a
Patient or potential Patient to ascertain if the Facility can adequately address those problems, meet
those needs, and to secure information for use in the development of the Individual Plan of Care.
H. Authorized Healthcare Provider. An individual authorized by law and currently licensed in
South Carolina as a Physician, advanced practice registered nurse, or physician assistant to provide
specific treatments, care, or services to Patients.
I. Blood Assay for Mycobacterium tuberculosis (‘‘BAMT’’). A general term to refer to in vitro diagnostic
tests that assess for the presence of tuberculosis (‘‘TB’’) infection with Mycobacterium tuberculosis . This
term includes, but is not limited to, IFN- g release assays (‘‘IGRA’’).
J. Chemical Dependency. A disorder manifested by repeated use of alcohol or another substance to
an extent that it interferes with a person’s health, social, or economic functioning; some degree of
habituation and dependence may be implied. May also be referred to as Substance Use Disorder.
K. Clinical Services Supervisor. The designated individual with responsibility for clinical supervi-
sion of treatment Staff and interpretation of program policy and standards.
L. Consultation. A meeting with a licensed Facility and individuals authorized by the Department
to provide information to Facilities in order to enable Facilities to better comply with the regulations.
M. Contact Investigation. Procedures that occur when a case of infectious Tuberculosis is identified,
including finding persons (contacts) exposed to the case, testing and evaluation of contacts to identify
Latent Tuberculosis Infection or Tuberculosis disease, and treatment of these persons, as indicated.
N. Controlled Substance. A medication or other substance included in Schedule I, II, III, IV, and
V of the Federal Controlled Substances Act or the South Carolina Controlled Substances Act.
O. Counselor. An individual licensed by the South Carolina Department of Labor, Licensing and
Regulation or certified as such by South Carolina Association of Alcoholism and Drug Abuse
Counselors.
P. Department. The South Carolina Department of Health and Environmental Control.
Q. Dietitian. An individual currently licensed as a Dietitian by the South Carolina Department of
Labor, Licensing and Regulation.
R. Direct Care Staff. Those individuals who provide care and services to the Patient.
S. Discharge. The point at which treatment, care, and services in a Facility are terminated and the
Facility no longer maintains active responsibility for the care of the Patient, except for Continuing Care
monitoring.
T. Elopement. An instance when a Patient who is physically, mentally, or chemically impaired
wanders, walks, runs away, escapes, or otherwise leaves the Facility unsupervised or unnoticed.
U. Exploitation. (1) Causing or requiring a Patient to engage in an activity or labor that is
improper, unlawful, or against the reasonable and rational wishes of a Patient. Exploitation does not
include requiring a Patient to participate in an activity or labor that is a part of a written individual
plan of care or prescribed or authorized by the Patient’s attending physician; (2) an improper,
unlawful, or unauthorized use of the funds, assets, property, power of attorney, guardianship, or
conservatorship of a Patient by an individual for the profit or advantage of that individual or another
individual; or (3) causing a Patient to purchase goods or services for the profit or advantage of the
seller or another individual through undue influence, harassment, duress, force, coercion, or swindling
by overreaching, cheating, or defrauding the Patient through cunning arts or devices that delude the
Patient and cause him or her to lose money or other property.
V. Facility for Chemically Dependent or Addicted Persons (Facility or Substance Use Disorder
Facility). A Facility organized to provide Outpatient or Residential Services to Chemically Dependent
or Addicted Persons and their families based on an Individual Plan of Care including diagnostic
treatment, individual and group counseling, family therapy, vocational and educational development
counseling, and referral services.
W. Follow-up. Intermittent contact with a Patient following discharge from the program, for
assessment of Patient status and needs.
X. Health Assessment. An evaluation of the health status of a staff member/volunteer by a
Physician, other Authorized Healthcare Provider, or a registered nurse. A registered nurse may
complete the Health Assessment pursuant to standing orders approved by a Physician as evidenced by
the Physician’s signature. The standing orders shall be reviewed annually by the Physician, with a copy
of the review maintained at the Facility.
Y. Individual Plan of Care. A written action plan based on assessment data that identifies the
Patient’s diagnosis and/or needs, the strategy for providing services to meet those needs, treatment
goals and objectives, and the criteria for terminating the specified interventions.
Z. In-process Counselor. A counselor accepted by the South Carolina Association of Alcoholism and
Drug Abuse Counselors as enrolled for certification.
AA. Inspection. A visit by the Department for the purpose of determining compliance with this
regulation.
BB. Intake. The administrative and assessment process for admission to a program.
CC. Interdisciplinary Team. A group designated by the Facility to provide or supervise care,
treatment, and services. The group normally includes but is not limited to the following persons:
Counselors, social workers, Physicians and other Authorized Healthcare Providers, pharmacists, peer
support specialists, etc.
DD. Investigation. A visit by Department representatives to a licensed or unlicensed entity for the
purpose of determining the validity of allegations received by the Department relating to statutory and
regulatory compliance.
EE. Legend Medications.
1. A Controlled Substance, when under federal law, is required, prior to being dispensed or
delivered to be labeled with any of the following statements:
a. ‘‘Caution: Federal law prohibits dispensing without prescription.’’
b. ‘‘Rx only’’; or
2. A Controlled Substance which is required by any applicable federal or state law to be
dispensed pursuant only to a prescription drug order or is restricted to use by practitioners only;
3. Any Controlled Substance considered to be a public health threat, after notice and public
hearing as designated by the South Carolina Board of Pharmacy; or
4. Any prescribed compounded prescription Controlled Substance within the meaning of the
South Carolina Pharmacy Practice Act.
FF. License. The authorization to operate a Substance Use Disorder Facility as defined in this
regulation and as evidenced by a certificate issued by the Department to a Facility.
GG. Licensed Nurse. A person to whom the South Carolina Board of Nursing has issued a license
as a registered nurse or licensed practical nurse, or an individual licensed as a registered nurse or
licensed practical nurse who resides in another state that has been granted multi-state licensing
privileges by the South Carolina Board of Nursing and may practice nursing in any Facility or activity
licensed by the Department subject to the provisions and conditions as indicated in the Nurse
Licensure Compact Act.
HH. Licensee. The individual, corporation, organization, or public entity licensed pursuant to this
regulation to provide dependency and Substance Use Disorder treatment services.
II. Medical Withdrawal Management Program. A program in a Residential Facility providing for
medically-supervised Withdrawal Management, with the capacity to provide screening for medical
complications of Substance Use Disorder, a structured program of counseling, if appropriate, and
referral for further rehabilitation.
JJ. Medication. A substance that has therapeutic effects, including, but not limited to, Legend, Non-
Legend, over-the counter, and nonprescription Medications, herbal products, vitamins, and nutritional
supplements.
KK. Medication Unit. A Satellite location established as part of, but geographically separate, from a
licensed Opioid Treatment Program to only administer Medications and conduct substance use
screening.
LL. Methadone. A synthetic opioid Medication usually administered on a daily basis.
MM. Minor. Any person whose age does not meet the criteria indicated in Section 101.C.
NN. Neglect. The failure or omission of a direct care staff member to provide the care, goods, or
services necessary to maintain the health or safety of a Patient including, but not limited to, food,
clothing, medicine, shelter, supervision, and medical services. Failure to provide adequate supervision
resulting in harm to Patients, including altercations or acts of assault between Patients, may constitute
neglect. Neglect may be repeated conduct or a single incident that has produced or could result in
physical or psychological harm or substantial risk of death. Noncompliance with regulatory standards
alone does not constitute neglect.
OO. Non-Legend Medications. A substance which may be sold without a prescription and which is
labeled for use by the consumer in accordance with state and federal law.
PP. Opioid Treatment Program. A program within an Outpatient Facility providing services using
Methadone or other opioid treatment Medication, and offering a range of treatment procedures and
services for the rehabilitation of persons dependent on opium, morphine, heroin, or any derivative or
synthetic Controlled Substance of that group.
QQ. Outpatient Facility. A Facility providing Outpatient Services.
RR. Outpatient Services. Non-Residential services for persons with Substance Use Disorder and/or
their families.
SS. Patient. Any individual who receives Outpatient or Residential Services from a licensed Facility.
TT. Physical Examination. An examination of a Patient by a Physician or other Authorized
Healthcare Provider which addresses those issues identified in Section 1100 of this regulation.
UU. Primary Counselor. An individual who is assigned by a Facility to develop, implement, and
periodically review the Patient’s Individual Plan of Care and to monitor a Patient’s progress in
treatment.
VV. Quality Improvement Program. The process used by a Facility to examine its methods and
practices of providing care services, identify the ways to improve its performance, and take actions that
result in improved quality of care for the Facility’s Patients.
WW. Repeat Violation. The recurrence of a violation cited under the same section of the regulation
within a twenty-four (24) month period.
XX. Residential Facility. A twenty-four (24) hour Facility offering Residential Treatment Program,
Medical Withdrawal Management, and Social Withdrawal Management services in a Residential setting
including services for parents with children.
YY. Residential Treatment Program. A program in a Residential Facility that is designed to
improve the Patient’s ability to structure and organize the tasks of daily living and foster recovery
through planned clinical activities, counseling, and clinical monitoring in order to promote successful
involvement or re-involvement in regular, productive daily activity, and, as indicated, successful
reintegration into family living.
ZZ. Revocation of License. An action by the Department to cancel or annul a Facility License by
recalling, withdrawing, or rescinding its authority to operate.
AAA. Satellite Facility. An approved Outpatient Facility at a location other than the main Outpa-
tient Facility that is owned or operated by the same licensee.
BBB. Self-Administration. A procedure by which any Medication is taken orally, injected, inserted,
or topically or otherwise administered by a Patient to himself or herself without prompting. The
procedure is performed without assistance and includes removing an individual dose from a previously
dispensed and labeled container (including a unit dose container), verifying it with the directions on
the label, taking it orally, injecting, inserting, or applying topically or otherwise administering the
Medication.
CCC. Social Withdrawal Management Program. A program in a Residential Facility providing
supervised Withdrawal Management in which neither the Patient’s level of intoxication nor physical
condition is severe enough to warrant direct medical supervision or the use of Medications to assist in
withdrawal, but which maintains medical backup and provides a structured program of counseling (if
appropriate), educational services, and referral for further rehabilitation.
DDD. Staff. Those individuals who are employees (full and part-time) of the Facility, to include
those individuals contracted to provide care and services for the Patients.
EEE. Substance Use Disorder. A recurrent use of alcohol or other substance causing clinically and
functionally significant impairment, such as health problems, disability, and failure to meet major
responsibilities at work, school, or home.
FFF. Suspension of License. An action by the Department requiring a Facility to cease operations
for a period of time or to require a Facility to cease admitting Patients, until such time as the
Department rescinds that restriction.
GGG. Tuberculosis Risk Assessment. An initial and ongoing evaluation of the risk for transmission
of Mycobacterium Tuberculosis in a particular healthcare setting. To perform a risk assessment, the
following factors shall be considered: the community rate of Tuberculosis, number of Tuberculosis
Patients encountered in the setting, and the speed with which Patients with Tuberculosis disease are
suspected, isolated, and evaluated. The Tuberculosis Risk Assessment determines the types of adminis-
trative and environmental controls and respiratory protection needed for a setting.
HHH. Volunteer. An individual who performs tasks that are associated with the operation of the
Facility without pay and at the direction of the Administrator or his or her designee.
III. Withdrawal Management. A process of withdrawing a Patient from a specific psychoactive
substance in a safe and effective manner.
102. License Requirements.
A. License. No person, private or public organization, political subdivision, or governmental agency
shall establish, operate, maintain, represent, advertise, or market itself as a Facility in South Carolina
without first obtaining a License from the Department. No Facility shall admit Patients prior to the
effective date of the License. When it has been determined by the Department that services for
Substance Use Disorder are being provided at a location, and the owner has not been issued a License
from the Department, the owner shall cease operation immediately and ensure the safety, health, and
well-being of the Patients. Current and/or previous violations of the South Carolina Code or
Department regulations may jeopardize the issuance of a License for the Facility or the licensing of any
other Facility or addition to an existing Facility that is owned/operated by the licensee. The Facility
shall provide only the treatment, services, and care it is licensed to provide pursuant to the definition
in Section 101.V. of this regulation. (I)
B. Compliance. An initial License shall not be issued to a proposed Facility until the Licensee has
demonstrated to the Department that the proposed Facility is in substantial compliance with the
licensing standards. In the event a current Licensee who already has a Facility or activity makes
application for another Facility, the currently licensed Facility /activity shall be in substantial compli-
ance with the applicable standards prior to the Department issuing a License to the proposed Facility
or amended License to the existing Facility. A paper or electronic copy of the licensing standards shall
be maintained at the Facility and accessible to all Staff members and Volunteers. Facilities shall comply
with applicable local, state, and federal laws, codes, and regulations.
C. Licensed Services. No Facility shall provide services outside the limits of the type Facility
identified on the face of the License and/or which the Facility has been authorized to provide. (I)
D. Satellite Facilities.
1. Outpatient Satellite locations, other than Medication Units, are authorized only in the same
county as the main Facility or in contiguous counties to the county in which the main Facility is
located.
2. Medication Units. A Licensed Outpatient Facility providing an Opioid Treatment Program
may establish a Medication Unit. A Medication Unit shall only administer Medications and conduct
substance use screening. Other required services shall be provided at the licensed Facility’s primary
location. The Medication Unit shall meet the regulatory requirements for Medication administration,
staffing, substance use screening, and construction.
a. Medication Units shall be opened no closer than forty-five (45) miles and no further than
ninety (90) miles from the primary Opioid Treatment Program.
b. The Facility shall obtain a registration from the Department’s Bureau of Drug Control and a
Controlled Substances registration from the federal Drug Enforcement Administration for each
Medication Unit.
c. The Facility shall not establish, operate, or maintain a Medication Unit without submitting
an application to and receiving approval from the Department. The Facility’s application for the
Medication Unit shall include documentation from the Department evidencing that the applicant
received either a Certificate of Need or a determination by the Department that Certificate of
Need review is not required.
E. Licensed Bed Capacity. No Residential Facility that has been authorized to provide a set number
of licensed beds, as identified on the face of the License, shall exceed the licensed bed capacity. No
Facility shall establish new care or services or occupy additional beds or renovated space without first
obtaining authorization from the Department. Licensed beds shall not be utilized by any individuals
other than Facility Patients. (I)
F. Persons Received in Excess of Licensed Bed Capacity. No Residential Facility shall receive for
treatment, care, or services persons in excess of the licensed bed capacity, except in cases of justified
emergencies (See Section 1400). (I)
G. Living Quarters for Staff in Residential Facilities. In addition to Patients, only Staff members,
Volunteers, or owners of the Facility and members of the owner’s immediate family may reside in
Facilities licensed under this regulation. Patient rooms shall not be utilized by any individuals other
than Facility Patients, nor shall bedrooms of Staff members or family members of the owner or the
Licensee be utilized by Patients. Staff members or family members of the owner or Licensee, or
Volunteers shall not use Patient living rooms, recreational areas, or dining rooms unless they are on
duty.
H. Issuance and Terms of License.
1. The License issued by the Department shall be posted by the Licensee in a conspicuous place
in a public area within the Facility.
2. The issuance of a License does not guarantee adequacy of individual care, services, personal
safety, fire safety, or the well-being of any Patient or occupant of a Facility.
3. A License is not assignable or transferable and is subject to revocation at any time by the
Department for the Licensee’s failure to comply with the laws and regulations of this state.
4. A License shall be effective for a specified Facility, at a specific location, for a specified period
following the date of issue as determined by the Department. A License shall remain in effect until
the Department notifies the Licensee of a change in the status.
5. Facilities owned by the same entity but which are not located on the same adjoining or
contiguous property shall be separately licensed. Roads or local streets, except limited access, shall
not be considered as dividing otherwise adjoining or contiguous property. For Facilities owned by
the same entity, separate Licenses are not required for separate buildings on the same or adjoining
grounds where a single type of service is provided.
6. Facilities providing Outpatient and Residential Services on the same premises shall be licensed
separately even though owned by the same entity.
I. Facility Name. No proposed Facility shall be named nor shall any existing Facility have its name
changed to the same or similar name as any other Facility licensed in South Carolina. The Department
shall determine if names are similar. If the Facility is part of a ‘‘chain operation’’ it shall then have the
geographic area in which it is located as part of its name.
J. Application. Applicants for a License shall submit to the Department a completed application on
a form prescribed, prepared, and furnished by the Department prior to initial licensing. Applicants for
a License shall file an application with the Department that includes an oath assuring the contents of
the application are accurate and true and in compliance with this regulation.
K. Required Documentation. The application for initial licensure shall include:
1. Completed application;
2. Proof of ownership of real property on which the Facility is located or a rental or lease
agreement allowing the Licensee to occupy the real property on which the Facility is located;
3. Verification of emergency evacuation plan (see Section 1401); and
4. Verification of Administrator’s qualifications.
L. Licensing Fees. Each applicant shall pay a License fee prior to the issuance of a License.
1. The initial and annual License fee shall be seventy-five dollars ($75.00) for Outpatient
Facilities. The initial and annual License fee for Outpatient Facility satellite locations shall be fifty
dollars ($50.00) per Satellite Facility.
2. For Residential Facilities, the annual License fee shall be ten dollars ($10.00) per bed or
seventy-five dollars ($75.00), whichever is greater.
M. Licensing Late Fees. Failure to submit a renewal application and fee to the Department by the
License expiration date shall result in a late fee of seventy-five dollars ($75.00) or twenty-five percent
(25%) of the licensing fee amount, whichever is greater, in addition to the licensing fee. Failure to
submit the licensing fee and licensing late fee to the Department within thirty (30) days of the licensure
expiration date shall render the Facility unlicensed. (II)
N. License Renewal. For a License to be renewed, applicants shall file an application with the
Department, pay a License fee, and shall not be under consideration for, or undergoing, enforcement
actions by the Department. Annual licensing fees shall also include any outstanding Inspection fees. All
fees are non-refundable, shall be made payable by check or credit card to the Department or online,
and shall be submitted with the application.
O. Amended License. No facility shall establish new care or services or occupy additional beds or
renovated space without first obtaining authorization from the Department. A Facility shall request
issuance of an amended License by application to the Department prior to any of the following
circumstances:
1. Change of licensed bed capacity;
2. Change of Facility location from one geographic site to another;
3. Changes in Facility name or address (as notified by the post office); or
4. Change in Facility service type.
P. Change of Licensee. A Facility shall request issuance of a new License by application to the
Department prior to any of the following circumstances:
1. A change in the controlling interest even if, in the case of a corporation or partnership, the
legal entity retains its identity and name; or
2. A change in the type of the legal entity, for example, sole proprietorship to or from a
corporation, partnership to or from a corporation, even if the controlling interest does not change.
Q. Variance. A variance is an alternative method that ensures the equivalent level of compliance
with the standards in this regulation. The Facility may request a variance to this regulation in a format
as determined by the Department. Variances shall be considered on a case by case basis by the
Department. The Department may revoke issued variances as determined to be appropriate by the
Department.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 100 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 200. ENFORCEMENT OF REGULATIONS
201. General.
The Department shall utilize Inspections, Investigations, Consultations, and other pertinent docu-
mentation regarding a proposed or licensed Facility in order to enforce this regulation.
202. Inspections and Investigations.
A. Inspections by the Department shall be conducted prior to initial licensing of a Facility and
subsequent Inspections conducted as deemed appropriate by the Department.
B. All Facilities are subject to Inspection and/or Investigation at any time without prior notice by
individuals authorized by the South Carolina Code of Laws. When Staff members and /or Patients are
absent, the Facility shall post information at the entrance of the Facility to those seeking legitimate
access to the Facility, including visitors. The posted information shall include contact information and
the expected time of return of the Staff members and Patients. The contact information shall include
the name of a designated contact and his or her telephone number. The telephone number for the
designated contact shall not be the Facility’s telephone number. (I)
C. Individuals authorized by South Carolina law shall be allowed to enter the Facility for the
purpose of Inspection and/or Investigation and granted access to all properties and areas, objects,
requested records, and documentation at the time of the Inspection or Investigation. The Department
shall have the authority to require the Facility to make photocopies of those documents required in the
course of Inspections or Investigations. Photocopies shall be used only for purposes of enforcement of
regulations and confidentiality shall be maintained except to verify the identity of individuals in
enforcement action proceedings. The physical area of Department Inspections and Investigations shall
be determined by the Department based on the potential impact or effect upon patients. (I)
D. When there is noncompliance with the licensing standards, the Facility shall submit an
acceptable plan of correction in a format determined by the Department. The plan of correction shall
be signed by the Administrator and returned by the date specified on the report of Inspection and/or
Investigation. The plan of correction shall describe: (II)
1. The actions taken to correct each cited deficiency;
2. The actions taken to prevent recurrences (actual and similar); and
3. The actual or expected completion dates of those actions.
E. In accordance with South Carolina Code Section 44–7–270, the Department may charge a fee
for Inspections.
1. Residential Facilities. The fee for initial, relocation, and routine Inspections shall be three
hundred fifty dollars ($350.00), plus twenty-five dollars ($25.00) per licensed bed. The Inspection fee
for a bed increase and/or service modification is two hundred dollars ($200.00), plus twenty-five
dollars ($25.00) per licensed bed. The fee for all follow-up Inspections shall be two hundred dollars
($200.00), plus twenty-five dollars ($25.00) per licensed bed.
2. Outpatient Facilities. The fee for initial, relocation, and routine Inspections shall be four
hundred fifty dollars ($450.00). The Inspection fee for service modification, including the establish-
ment of a Satellite Facility, and follow-up Inspections is two hundred fifty dollars ($250.00).
F. The Licensee shall pay the following Inspection fees during the construction phase of the
project. The plan Inspection fee is based on the total estimated cost of the project whether new
construction, an addition, or a renovation. The fees are detailed in the table below.

Construction Inspection Fees 
Plan Inspection 
Total Project Cost Fee 
¢ $10,001 $750 
$10,001 - $100,000 $1,500 
$100,001 - $500,000 $2,000 
$ $500,000 $2,500 plus $100 for each addi-
tional $100,000 in project cost 
Site Inspection 
50% Inspection $500 
80% Inspection $500 
100% Inspection $500 
203. Consultations.
Consultations shall be provided by the Department as requested by the Facility or as deemed
appropriate by the Department.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 200 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 300. ENFORCEMENT ACTIONS
301. General.
When the Department determines that a Facility is in violation of any statutory provision or
regulation relating to the operation or maintenance of such Facility, the Department, upon proper
notice to the Licensee, may deny, suspend, or revoke Licenses, or assess a monetary penalty, or both.
302. Violation Classifications.
A. Violations of standards in this regulation are classified as follows:
1. Class I violations are those that present an imminent danger to the health, safety, or well-being
of the persons in the Facility or a substantial probability that death or serious physical harm could
result therefrom. A physical condition or one or more practices, means, methods, or operations in
use in a Facility may constitute such a violation. The condition or practice constituting a Class I
violation shall be abated or eliminated immediately unless a fixed period of time, as stipulated by the
Department, is required for correction. Each day such violation exists after expiration of the time
established by the Department shall be considered a subsequent violation.
2. Class II violations are those, other than Class I violations, that have a negative impact on the
health, safety, or well-being of persons in the Facility. The citation of a Class II violation shall specify
the time within which the violation is required to be corrected. Each day such violation exists after
expiration of this time shall be considered a subsequent violation.
3. Class III violations are those that are not classified as Class I or II in this regulation or those
that are against the best practices. The citation of a Class III violation shall specify the time within
which the violation is required to be corrected. Each day such violation exists after expiration of this
time shall be considered a subsequent violation.
B. The notations, ‘‘(I)’’ or ‘‘(II),’’ placed within sections of this regulation, indicate those standards
are considered Class I or II violations if they are not met, respectively. Failure to meet standards not so
annotated are considered Class III violations.
C. In determining an enforcement action, the Department shall consider the following factors:
1. Specific conditions and their impact or potential impact on health, safety, or well-being of the
Patients including, but not limited to:
a. Deficiencies in Medication management; critical waste water problems; housekeeping, or fire
and life safety-related problems that pose a health threat to the Patients;
b. Power, water, gas, or other utility and/or service outages;
c. Patients exposed to air temperature extremes that jeopardize their health;
d. Unsafe condition of the building or structure;
e. Indictment of an Administrator for malfeasance or a felony, which by its nature indicates a
threat to the Patients;
f. Direct evidence of Abuse, Neglect, or Exploitation;
g. Lack of food or evidence that the Patients are not being fed properly;
h. No Staff available at the Facility with Patients present;
i. Unsafe procedures and/or treatment being practiced by Staff; (I)
2. Repeated failure of the Licensee or Facility to pay assessed charges for utilities and/or services
resulting in repeated or ongoing threats to terminate the contracted utilities and/or services; (II)
3. Efforts by the Facility to correct cited violations;
4. Overall conditions of the Facility;
5. History of compliance; and
6. Any other pertinent conditions that may be applicable to current statutes and regulations.
D. When imposing monetary penalties, the Department may invoke South Carolina Code Section
44–7–320(C) to determine the dollar amount or may utilize the following schedule:
FREQUENCY CLASS I CLASS II CLASS III
1st $ 500–1,500 $ 300–800 $100–300
2nd 1,000–3,000 500–1,500 300–800
3rd 2,000–5,000 1,000–3,000 500–1,500
4th 5,000 2,000–5,000 1,000–3,000
5th 5,000 5,000 2,000–5,000
6th 5,000 5,000 5,000
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 300 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 400. POLICIES AND PROCEDURES (II)
A. The Facility shall maintain and adhere to written policies and procedures addressing the
manner in which the requirements of this regulation shall be met. The Facility shall be in full
compliance with the policies and procedures.
B. The written policies and procedures shall include the following:
1. Staffing and training;
2. Reporting incidents, accidents, reportable diseases, closure and zero census;
3. Patient records;
4. Admission and Discharge;
5. Patient care, treatment, and services;
6. Medication management;
7. Maintenance including doors, windows, heating, ventilation, air conditioning, fire alarm,
electrical, mechanical, plumbing, and for all equipment;
8. Infection control and housekeeping;
9. Quality Improvement Program; and
10. Fire Prevention;
C. The Facility shall establish a time period for review, not to exceed two (2) years, of all policies
and procedures, and such reviews shall be documented and signed by the Administrator. All policies
and procedures shall be accessible to Facility staff, printed or electronically, at all times.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 400 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 500. STAFF AND TRAINING
501. General (II).
A. The Facility shall develop and implement policies and procedures to provide for appropriate
Staff and/or Volunteers in numbers and training to suit the needs and condition of the Patients and
meet the demands of effective emergency on-site action that might arise. Training requirements/quali-
fications for the tasks each performs shall be in compliance with all local, state, and federal laws, and
current professional organizational standards.
B. The Facility shall maintain accurate information regarding all Staff and/or Volunteers of the
Facility. The documentation shall include at least current address, phone number, health and work
and/or training background, as well as current information. The Facility shall ensure all employees are
assigned certain duties and responsibilities that shall be in writing and in accordance with the
individual’s capability. (II)
C. When a Facility engages a source other than the Facility to provide services normally provided
by the Facility, the Facility shall maintain documentation of the written agreement with the source that
describes how and when the services are to be provided, the exact services to be provided, and that
these services are to be provided by qualified individuals. The source shall comply with this regulation
in regard to Patient care, services, and rights.
D. The Facility shall maintain documentation to ensure the Facility meets staffing requirements in
Sections 503, 504, and 505.
502. Administrator (II).
A. Each Facility shall have a full-time Administrator who is responsible for the overall management
and operation of the Facility and has at least a bachelor’s degree in a related field.
B. A Staff member shall be designated by name or position, in writing, to act in the absence of the
Administrator, for example, a listing of the lines of authority by position title, including the names of
the individuals filling these positions.
503. Staffing for Residential Facilities (I).
A. All Staff members and/or Volunteers on duty shall be present, awake, and dressed at all times
when Patients are present in the Facility. All Staff members and/or Volunteers shall know how to
respond to Patient needs and emergencies.
B. Additional Staff shall be provided if it is determined that the minimum Staff requirements are
inadequate to provide appropriate services and supervision to the Patients of a Facility.
C. Staffing for Residential Treatment Programs.
1. The number of Staff members that shall be maintained in all Facilities:
a. In each building, there shall be at least one (1) Staff member and/or Volunteer on duty for
each ten (10) Patients or fraction thereof present from 7:00 am until 7:00 p.m.
b. In each building, there shall be at least one (1) Staff member and/or Volunteer for each
twenty (20) Patients or fraction thereof from 7:00 p.m. until 7:00 a.m.
2. The Facility shall have at least one (1) Physician available during Facility operating hours,
either in person or by telephone for consultation and for emergencies.
D. Staffing for Withdrawal Management Programs.
1. In each building, there shall be at least one (1) Direct Care or Counselor Staff member for
each ten (10) Patients or fraction thereof on duty at all times.
2. In Residential Facilities providing Medical Withdrawal Management, Staff members and
Volunteers shall be under the general supervision of a Physician or registered nurse; a Physician,
Licensed Nurse, or other Authorized Healthcare Provider shall be present at all times.
505. Staffing for Opioid Treatment Programs (I).
A. The Opioid Treatment Program Physician shall have authority over all medical aspects of care
and make treatment decisions in consultation with treatment Staff consistent with the needs of the
Patient, clinical protocols, and research findings. The Facility shall have at least one (1) Physician
available during dosing and Facility operating hours, either in person or by telephone for consultation
and for emergencies.
B. The Facility shall have a pharmacist or other person licensed to dispense Opioid Treatment
Program Medications pursuant to the South Carolina Code of Laws who is responsible for dispensing
the amounts of Opioid Treatment Program Medications administered and shall record and counter-
sign all changes in dosing schedules.
C. The Facility shall have one (1) Licensed Nurse present at all times Medications are being
administered to Patients.
D. The Opioid Treatment Program shall have a least one (1) full-time counselor on staff for every
fifty (50) Patients or fraction thereof. Counselors shall be qualified as specified in Section 508.
506. Inservice Training (II).
A. All Facilities shall provide Staff and Volunteers the necessary training to perform the duties for
which they are responsible in an effective manner. The Facility shall require all Staff members and
Volunteers to complete the necessary training to perform their duties and responsibilities. The Facility
shall document all in-service training. Staff training shall be signed and dated by the individual
providing the training and the person receiving the training. The signature for the individual
providing the training may be omitted for online training.
B. All Facilities shall provide the following training to all Staff and Volunteers prior to Patient
contact and at a frequency as determined by the Facility, but at least annually:
1. The nature of Substance Use Disorder, complications of Chemical Dependency, and withdraw-
al symptoms.
2. Confidentiality of Patient information and records and the protection of Patient rights.
C. All Residential Facilities shall provide the following training to all Staff and Volunteers prior to
Patient contact and at a frequency as determined by the Facility, but at least annually:
1. Cardio-pulmonary resuscitation to ensure that there is at least one (1) certified individual
present when Patients are in the Facility;
2. Basic first-aid to include emergency procedures as well as procedures to manage and/or care
for minor accidents or injuries;
3. Procedures for checking and recording vital signs;
4. Management/care of persons with contagious and/or communicable disease;
5. Medication management;
6. Use of restraints and seclusion;
7. Seizure response training; and
8. OSHA standards regarding bloodborne pathogens.
D. All Opioid Treatment Programs shall provide opioid Medication treatment training to all Staff
and Volunteers prior to Patient contact and at a frequency as determined by the Facility, but at least
annually.
E. All Staff members and Volunteers shall have documented orientation to the purpose and
environment of the Facility within twenty-four (24) hours of their first day on the job in the Facility.
507. Health Status (I).
A. All Staff and Volunteers who have contact with Patients, including food services Staff and
Volunteers, shall have a Health Assessment, as defined in Section 101.X, within twelve (12) months
prior to initial Patient contact. The Health Assessment shall include tuberculin skin testing as described
in Section 1702.
B. For Staff members and/or Volunteers working at multiple Facilities operated by the same
Licensee, the documented Health Assessment shall be accessible at each Facility, provided the
information is in compliance with this regulation.
508. Counselors (II).
A. Each Facility shall have at least one (1) Staff Counselor who is fully-certified or licensed. All non-
certified and/or licensed Counselors shall be under the direct supervision of an on-site fully-certified or
licensed Counselor.
B. Staff and Volunteers providing clinical counseling services shall have one (1) of the following
qualifications:
1. Certification:
a. Certification under the system administered by the South Carolina Association of Alcohol
and Drug Abuse Counselors Certification Commission, or currently engaged, as verified and
documented in the individual’s personnel file, in the South Carolina Association of Alcohol and
Drug Abuse Counselors certification process that is to be completed within a three (3)-year period
from date of hire as a Counselor; or
b. Certification as a Counselor by:
(1) The National Association of Alcohol and Drug Abuse Counselors;
(2) An International Certification Reciprocity Consortium-approved certification board; or
(3) Any other South Carolina Department of Alcohol and Other Drug Abuse Services -
approved credentialing or certification association or commission; or
2. Licensure:
a. Licensed as a Psychiatrist by the South Carolina Board of Medical Examiners;
b. Licensed as a Psychologist by the South Carolina Board of Examiners in Psychology;
c. Licensed as a Social worker by the South Carolina Board of Social Work Examiners; or
d. Licensed as a Counselor or therapist by the South Carolina Board of Examiners for
Licensure of Professional Counselors, Marriage and Family Therapists, Addiction Counselors and
Psycho-Educational Specialists, pursuant to Section 40–75–30, of the South Carolina Code of Laws,
1976.; or
3. Licensure as a Licensed Addiction Counselor Associate by the South Carolina Board of
Examiners for Licensure of Professional Counselors, Marriage and Family Therapists, Addiction
Counselors and Psycho-Educational Specialists, pursuant to Section 40–75–30, of the South Carolina
Code of Laws, 1976, under appropriate supervision. Full licensure must be completed within a three
(3)-year period from date of hire as a Counselor.
C. Counselors in Opioid Treatment Programs shall have one (1) of the following qualifications:
1. Any of the certifications or licensures in 508.B above; or
2. The American Academy of Health Care Providers in the Addictive Disorders; or
3. The National Board for Certified Counselors; or
4. Any other equivalent, nationally-recognized, and South Carolina Department of Alcohol and
Other Drug Abuse Services-approved association or accrediting body that includes similar competen-
cy-based testing, supervision, educational, and substantial experience.
D. In Facilities providing prevention services, Counselors shall have one (1) of the following
qualifications:
1. Certification by the South Carolina Association of Prevention Professionals and Advocates as a
Prevention Professional or Senior Prevention Professional; or
2. In-process of becoming certified as a Prevention Professional. This certification shall be
achieved within a thirty-six (36)-month period of time from the date of hire as a prevention
Counselor.
E. Any individual employed as a direct Patient Counselor, Opioid Treatment Program Counselor,
or prevention services professional, to include contracted Staff, who does not obtain his or her
certification or licensing within the above time-periods, shall cease providing counseling services until
that certification or licensing status is achieved.
F. The Facility shall verify and maintain documentation of each Counselor’s qualifications in the
individual’s Staff record.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 500 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 600. REPORTING
601. Accidents and Incidents (II).
A. The Facility shall maintain a record of each accident and/or incident, including usage of
mechanical and/or physical restraints, involving Patients, Staff members or Volunteers, occurring in the
Facility or on the Facility grounds. The Facility shall retain all documented incidents reported
pursuant to this section six (6) years after the Patient stops receiving services at the Facility.
B. The Facility shall report the following types of incidents to the next of kin or responsible party
at the earliest practicable hour, not exceeding twenty-four (24) hours of the incident. The Facility shall
report the following types of incidents to the Department immediately, not to exceed twenty-four (24)
hours, via the Department’s electronic reporting system or as otherwise determined by the Depart-
ment. incidents requiring reporting include, but are not limited to:
1. Confirmed or Suspected Abuse, Neglect or Exploitation against a Patient by Facility Staff;
2. Crimes committed against Patients;
3. Death: For Residential Facilities, any Patient’s death in the Facility or on the Facility grounds;
for Opioid Treatment Programs, any Patient’s death regardless of location;
4. Overdose reversal (naloxone);
5. Elopement (Residential Facility only);
6. Bone fracture or joint fracture;
7. Hospitalization as a result of accident and/or incident;
8. Medication Error;
9. Attempted Suicide; and
10. Severe injury involving use of restraint.
C. The Facility shall submit a separate written investigation report within five (5) days of every
incident required to be immediately reported to the Department pursuant to Section 601.B via the
Department’s electronic reporting system or as otherwise determined by the Department. Reports
submitted to the Department shall contain only: Facility name, License number, type of accident
and/or incident, the date of accident and/or incident occurred, number of Patients directly injured or
affected, Patient medical record identification number, Patient age and sex, number of Staff directly
injured or affected, number of visitors directly injured or affected, witness(es) name(s), identified cause
of accident and/or incident, internal investigation results if cause unknown, a brief description of the
accident and/or incident including location where occurred, and treatment of injuries.
602. Fire and Disasters (II).
A. The Facility’s Administrator or his or her designee shall notify the Department immediately via
telephone, e-mail, or fax of any fire in the Facility. The Facility shall submit a complete written report
to include fire reports within a time-period determined by the Facility, but not to exceed forty-eight
(48) hours from the occurrence of the fire.
B. The Facility’s Administrator, or his or her designee, shall notify the Department immediately of
any natural disaster or fire that requires displacement of the Patients, or jeopardizes or potentially
jeopardizes the safety of the Patients. The Facility shall submit a complete written report that includes
the fire report from the local fire department within a time-period as determined by the Facility, but
not to exceed forty-eight (48) hours.
603. Communicable Diseases and Animal Bites (I).
The Facility shall report all cases of diseases and animal bites that are required to be reported to the
appropriate county health department in accordance with R.61–20, Communicable Diseases.
604. Administrator Change.
The Licensee shall notify the Department via email, or a means as otherwise determined by the
Department within seventy-two (72) hours of any change in Administrator status. The Licensee shall
provide the Department in writing within ten (10) days the name of the newly-appointed Administra-
tor and the effective date of the appointment.
605. Joint Annual Report.
Residential Facilities providing a Medical Withdrawal Management Program and Outpatient Facili-
ties providing an Opioid Treatment Program, shall complete and return a ‘‘Joint Annual Report’’ to
the South Carolina Revenue and Fiscal Affairs Office within the time-period specified by the
Department.
606. Accounting of Controlled Substances (I).
Any Facility registered with the Department’s Bureau of Drug Control and the federal Drug
Enforcement Agency shall report any theft or loss of Controlled Substances to local law enforcement
and to the Department’s Bureau of Drug Control within seventy-two (72) hours of the discovery of the
loss and/or theft. Any Facility permitted by the South Carolina Board of Pharmacy shall report the loss
or theft of drugs or devices in accordance with Section 40–43–91 of the South Carolina Code of Laws.
607. Facility Closure.
A. Prior to the permanent closure of a Facility, the Licensee shall notify the Department in writing
of the intent to close and the effective closure date. Within ten (10) days of the closure, the Facility shall
notify the Department of the provisions for the maintenance of the records, the identification of those
Patients displaced, the relocated site, and the dates. On the date of closure, the License shall be
returned to the Department.
B. In instances where a Facility temporarily closes, the Licensee shall notify the Department in
writing within fifteen (15) calendar days prior to temporary closure. In the event of temporary closure
due to an emergency, the Facility shall notify the Department within twenty-four (24) hours of the
closure via telephone, email, or fax. At a minimum this notification shall include, but not be limited to:
the reason for the temporary closure, the location where the Patients have been and/or will be
transferred, the manner in which the records are being stored, and the anticipated date for re-
opening.
C. The Department shall consider, upon appropriate review, the necessity of inspecting and
determining the applicability of current construction standards of the Facility prior to its reopening. If
the Facility is closed for a period longer than one (1) year, and there is a desire to re-open, the Facility
shall re-apply to the Department for licensure and shall be subject to all licensing requirements at the
time of that application, including construction-related requirements for a new Facility.
608. Zero Census.
In instances when there have been no Patients in a Facility for any reason for a period of ninety (90)
days or more, the Facility shall notify the Department in writing that there have been no admissions,
no later than the one hundredth (100
th) calendar day following the date of departure of the last active
Patient. At the time of that notification, the Department shall consider, upon appropriate review of the
situation, the necessity of inspecting the Facility prior to any new and/or readmissions to the Facility. In
the event the Facility is at zero census or temporarily closed, the Licensee is still required to apply and
pay the licensing fee to keep the License active. If the Facility has no Patients for a period longer than
one (1) year and there is a desire to admit a Patient, the Facility shall re-apply to the Department for
licensure and shall be subject to all licensing requirements at the time of that application, including
construction-related requirements for a new Facility.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 600 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 700. PATIENT RECORDS
701. Content (II).
A. The Facility shall initiate and maintain a Patient record for every individual screened, assessed
and/or treated. The record shall contain sufficient information to identify the Patient and the agency
and/or person responsible for each Patient, support the diagnosis, justify the treatment, and describe
the response and/or reaction to treatment. The record contents shall also include the provisions for
release of information, Patient rights, consent for treatment (approval by parent and/or guardian of
Patient), Medications prescribed and administered, and diet (Residential Facilities only), documenta-
tion of the course and results, and promote continuity of treatment among treatment providers,
consistent with acceptable standards of practice. In Facilities providing services for Parents with
children, the name and age of each child shall be maintained in the Facility. All entries shall be written
legibly in ink, typed, or electronic media, and signed and dated or documented in the electronic
medical record.
B. If the Facility permits any portion of a Patient’s record to be generated by electronic or optical
means, there shall be policies and procedures to prohibit the use or authentication by unauthorized
users.
C. Specific entries and documentation shall include at a minimum:
1. Consultations by Physicians or other Authorized Healthcare Providers;
2. Signed and dated orders and recommendations for all Medication, care, services, and diet
(Residential Facilities only) from Physicians or other Authorized Healthcare Providers, which shall be
completed prior to, or at the time of admission, and subsequently, as warranted; (I)
3. Intake screening and initial physical assessment completed by the nurse or Counselor;
4. A signed and dated original consent for treatment; (I)
5. The report of the mental status examination and other mental health assessments as defined
in Section 101.G. as appropriate;
6. Notes of counseling sessions and any other changes in the Patient’s mental and physical
condition; and
7. Medication management and administration, and treatment records.
8. Discharge summary, completed within a time-period as determined by the Facility, but no
later than three (3) business days, and shall include at minimum:
a. Time and circumstances of Discharge or transfer, including condition at Discharge or
transfer, or death; and
b. The recommendations and arrangements for further treatments, including Aftercare.
D. Electronic signatures may be used in the Patient record if they are in accordance with applicable
laws and regulations, and require a signature. Electronic authorization shall be limited to a unique
identifier (confidential code) used only by the individual making the entry to preclude the improper or
unauthorized use of any electronic signature
702. Screening (I).
A. The Facility shall have written protocols for screening individuals presenting for admission. The
Facility shall maintain documentation of the rationale for the denial of admission and referral of the
individual as applicable.
B. All screening shall be documented for each individual presenting to the Facility.
C. For Facilities providing a Medical Withdrawal Management Program, the Intake screening shall
be conducted by a Physician or other Authorized Healthcare Provider to determine the need for
medical services or referral for serious medical complications.
D. For Facilities providing Social Withdrawal Management, the Intake screening shall be provided
by Staff or Volunteers trained to monitor the Patient’s physical condition.
E. For Facilities providing an Opioid Treatment Program, screening shall include:
1. Evidence of tolerance to an opioid;
2. History of physiological dependence for at least one (1) year prior to admission. The Opioid
Treatment Program Physician may waive the one (1)-year history of dependence when the Patient
seeking admission meets one (1) of the following criteria:
a. The Patient has been recently released from a penal or chronic care Facility with a high risk
of relapse;
b. The Patient has been previously treated and is at risk of relapse;
c. The Patient is pregnant and does not exhibit objective signs of opioid withdrawal or
physiological dependence;
3. Evidence of multiple and daily self-administration of an opioid;
4. Reasonable attempts to confirm that the applicant is not enrolled in one (1) or more other
Opioid Treatments Programs;
5. Controlled Substance history to determine dependence on opium, morphine, heroin, or any
derivative or synthetic controlled substance of that group. The substance history shall include:
a. Controlled Substance(s) utilized;
b. Frequency of use;
c. Amount utilized;
d. Duration of use;
e. Age when first utilized;
f. Route of administration;
g. Previous treatment(s);
h. Unsuccessful efforts to control use; and
i. Inappropriate use of prescribed opioids.
703. Assessment for Residential Treatment Programs (II).
A written assessment of the Patient in accordance with Section 101.G shall be conducted by a
designated Counselor as evidenced by his or her signature and date within a time-period determined
by the Facility, but no later than five (5) business days after admission.
704. Assessment for Withdrawal Management Programs (II).
A written clinical Assessment of the Patient completed by a Licensed Nurse as evidenced by his or
her signature and date in accordance with Section 101.G shall be conducted prior to the delivery of
treatment. The clinical Assessment shall include a review of the Patient’s Controlled Substance
misuse/usage and treatment history.
705. Bio-Psycho-Social Assessment for Opioid Treatment Program (II).
A comprehensive Bio-Psycho-Social Assessment shall be completed by the Patient’s primary Counsel-
or once the Patient is stabilized but not later than thirty (30) calendar days following admission. The
Assessment shall include:
A. A description of the historical course of the Chemical Dependence to include substances of
misuse such as alcohol and tobacco, amount, frequency of use, duration, potency, and method of
administration, previous withdrawal from Opioid Treatment Program Medication and/or treatment
attempts, and any psychological or social complication.
B. A health history regarding chronic or acute medical conditions, such as HIV, STDs, hepatitis (B,
C, D), TB, diabetes, anemia, sickle cell trait, pregnancy, chronic pulmonary diseases, and renal
diseases.
C. Information related to the family of the Patient.
706. Individual Plan of Care (II).
The Facility shall develop an Individual Plan of Care with participation by the Patient or responsible
party and Interdisciplinary Team as evidenced by their signatures and dates. The Individual Plan of
Care shall contain specific goal-related objectives based on the needs of the Patient as identified during
the Assessment phase, including adjunct support service needs and other special needs. The Individual
Plan of Care shall also include the methods and strategies for achieving these objectives and meeting
these needs in measurable terms with expected achievement dates. The type and frequency of
counseling, as well as Counselor assignment, shall be included. The criteria for terminating specified
interventions shall be included in the Individual Plan of Care. Individual Plan of Care shall be
reviewed on a periodic basis as determined by the Facility and/or revised as changes in Patient needs
occur.
A. In Residential Treatment Programs, an Individual Plan of Care shall be completed no later than
seven (7) calendar days after admission.
B. For a Residential Facility offering a Withdrawal Management Program, an Individual Plan of
Care shall be completed for supervised withdrawal within a time-period determined by the Facility’s
policies and procedures, but no later than seven (7) business days after admission.
707. Individual Plan of Care for Opioid Treatment Program (II).
A. The Facility shall develop and document an Individual Plan of Care within thirty (30) calendar
days of admission with participation by the Patient and the primary Counselor.
B. The primary Counselor shall review the Patient progress in treatment and accomplishment of
Individual Plan of Care goals not less than every ninety (90) calendar days during the first year of
treatment and every six (6) months thereafter. The Counselor and Patient or responsible party shall
sign and date any changes.
708. Record Maintenance.
A. The Licensee shall provide accommodations, space, supplies, and equipment for the protection,
storage, and maintenance of Patient records. Patient records shall be stored in an organized manner.
B. The Patient record is confidential and shall be made available only to individuals authorized by
the Facility and in accordance with local, state, and federal laws, codes, and regulations. (II)
C. The Facility shall maintain records generated by organizations or individuals contracted by the
Facility for care or services.
D. Upon Discharge of a Patient, the record shall be completed within thirty (30) calendar days and
filed in an inactive or closed file maintained by the Licensee.
E. Records of adult Patients may be destroyed after six (6) years following Discharge of the Patient.
Records of Minors shall be retained for six (6) years or until majority, whichever period of time is
greater. Other regulation-required documents, e.g., Medication destruction, fire drills, etc., shall be
retained for at least twelve (12) months or since the last Department routine Inspection, whichever is
the longer period.
F. Records of current Patients are the property of the Facility and shall be maintained at the
Facility and shall not be removed without court order.
G. In the event of change of ownership, all active Patient records or copies of active Patient records
shall be transferred to the new owner(s).
H. When a Patient transfers from one licensed Facility to another within the provider network
(same Licensee) the original record may follow the Patient; the sending Facility shall maintain
documentation of the Patient’s transfer and/or Discharge dates and identification information.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 700 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 800. ADMISSION (I)
801. General.
Individuals seeking admission shall be identified as appropriate for the level of care or services,
treatment, or procedures offered. The Facility shall establish admission criteria that are consistently
applied and comply with state and federal laws and regulations. The Facility shall admit only those
persons whose needs can be met within the accommodations and services provided by the Facility.
802. Residential Facilities.
A. Residential Facilities shall not admit any person who, because of acute mental illness or
intoxication, presents an immediate threat of harm to him or herself and/or others
B. Parental consent shall be obtained for all persons under eighteen (18) years of age prior to
admission to a Residential Facility. If any court of competent jurisdiction declares a person under
eighteen (18) years of age an emancipated Minor, such person may be admitted to the Facility without
parental consent.
C. Residential Treatment Programs shall not admit any person needing Withdrawal Management
services, hospitalization, or nursing home care.
D. Withdrawal Management Programs.
1. Appropriate admission to a Facility providing Withdrawal Management shall be determined by
a licensed or certified Counselor and subsequently shall be authorized by a Physician or other
Authorized Healthcare Provider in accordance with Section 1100.
2. Withdrawal Management Programs shall not admit any person needing hospitalization,
Residential Treatment Program, or nursing home care.
3. Parental consent shall be obtained for all persons under eighteen (18) years of age prior to
admission to a Residential Treatment Program. If any court of competent jurisdiction declares a
person under eighteen (18) years of age an emancipated Minor, then such person may be admitted
to the program without parental consent.
803. Opioid Treatment Programs.
A. Persons shall not be admitted to the Opioid Treatment Program to receive opioids for pain
management only. Appropriate referrals by the Opioid Treatment Program Physician shall be made as
necessary, e.g., pain management specialist.
B. No person under eighteen (18) years of age shall be admitted to an Opioid Treatment Program
unless a parent, legal guardian, or responsible adult consents in writing to such treatment.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 800 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 900. PATIENT CARE, TREATMENT, AND SERVICES
901. General.
A. The Facility shall provide Patient care and services, including routine and emergency medical
care, as identified in the Patient record and as ordered by a Physician or other Authorized Health Care
Provider. Care and services shall be provided and coordinated among those responsible during the
treatment process and modified as warranted based on any changing needs of the Patient, and detailed
in the Individual Plan of Care. (I)
B. Care, treatment, and services shall be rendered effectively and safely in accordance with orders
from Physicians, other Authorized Healthcare Providers, and certified and/or licensed Counselors, and
precautions taken for Patients with special conditions, e.g., pacemakers, wheelchairs, etc. (I)
C. The Facility shall document that Patients were offered the opportunity to participate in
Aftercare and/or Continuing Care programs offered by the Facility or through referral. (II)
D. In the event of closure of a Facility for any reason, the Facility shall ensure continuity of
treatment and/or care by promptly notifying the Patient’s attending Physician or other Authorized
Healthcare Provider or Counselor and arranging for referral to other Facilities at the direction of the
Physician or other Authorized Healthcare Provider or Counselor. The facility shall document the
notification and referral in the Patient’s medical record.
902. Residential Facilities. (II)
A. Patients shall receive assistance in activities of daily living as documented in the Individual Plan
of Care.
B. Patients shall be provided necessary items and assistance to maintain their personal hygiene.
C. Opportunities shall be provided for participation in religious services. Assistance in obtaining
pastoral counseling shall be provided upon request by the Patient.
D. Precautions shall be taken for the protection of the personal possessions of the Patients,
including their personal funds. The Facility may secure the personal funds of the Patient provided the
Patient authorizes the Facility to do so. The Facility shall maintain an accurate accounting of the funds,
including evidence of purchases by Facility on behalf of the Patients. No personal monies shall be given
to anyone, including family members, without written consent of the Patient. If money is given to
anyone by the Facility, a receipt shall be obtained.
E. Residential Treatment Programs shall document in the Patient’s medical record that the Facility
has provided or made available the following:
1. Specialized professional consultation, supervision, and direct affiliation with other levels of
treatment;
2. Arrangements for appropriate laboratory and toxicology tests as needed;
3. Counselors to assess and treat Patients for Substance Use Disorders and obtain and interpret
information regarding the needs of the Patients;
4. Counselors to provide a planned regimen of twenty-four (24) hour professionally-directed
evaluation, care, and treatment services for persons with Substance Use Disorders and their families
to include individual, group, and/or family counseling directed toward specific Patient goals
indicated in his or her Individual Plan of Care;
5. Educational guidance and educational program referral when indicated; and
6. Vocational counseling for any Patient when indicated. For those not employed, Staff and/or
Volunteers shall facilitate the Patient’s pursuit of employment search;
F. Withdrawal Management Programs.
1. Facilities Offering a Medical Withdrawal Management Program shall document in the Patient’s
medical record that the facility has provided the following:
a. Continuing observation and monitoring of each Patient’s condition to recognize and
evaluate significant signs and symptoms of medical distress and take appropriate action. Each
Patient’s general condition, including vital signs, shall be documented at a frequency as deter-
mined by the Facility, but not less than three (3) times during the first seventy-two (72) hours of
admission to the Facility;
b. A plan for supervised withdrawal, to be implemented upon admission;
c. Counseling designed to motivate Patients to continue in the treatment process and referral
to the appropriate treatment modality.
2. Facilities offering a Social Withdrawal Management Program shall document in the Patient’s
medical record that the Facility has provided the following:
a. Development of an Individual Plan of Care for supervised withdrawal;
b. Continuing observation of each Patient’s condition to recognize and evaluate significant
signs and symptoms of medical distress and take appropriate action; and
c. Counseling designed to motivate Patients to continue in the treatment process.
3. Facilities providing a Withdrawal Management Program shall provide room, dietary service,
care, and supervision necessary for the maintenance of the Patient.
903. Facilities Providing an Opioid Treatment Program.
A. Services (II).
1. Services shall be directed toward reducing or eliminating the use of illicit Controlled
Substances, criminal activity, or the spread of infectious disease while improving the quality of life
and functioning of the Patient. Opioid Treatment Programs shall follow rehabilitation stages in
sufficient duration to meet the needs of the Patient. These stages include initial treatment, early
stabilization, long-term treatment, medical maintenance, and immediate emergency treatment when
needed.
2. The Opioid Treatment Program shall directly provide, contract, or make referrals, for services
based upon the needs of the Patient.
3. As part of Substance Use Disorder rehabilitative services provided by the Opioid Treatment
Program, each Patient shall be provided with individual, group, and family counseling as based on
needs identified during the assessment. The frequency and duration of counseling provided to
Patients shall be determined by the needs of the Patient and be consistent with the Individual Plan of
Care. Counseling shall address, as a minimum:
a. Treatment and recovery objectives included in the Individual Plan of Care, as well as
education regarding HIV, Hepatitis, and other infectious diseases. HIV testing shall be made
available as appropriate, while maintaining Patient confidentiality;
b. Concurrent substance misuse;
c. Involvement of family and significant others with the informed consent of the Patient;
d. Providing treatment groups; and
e. Guidance in seeking alternative therapies, if applicable.
B. Support Services.
1. The Opioid Treatment Program shall ensure that a comprehensive range of support services,
including, but not limited to, vocational, educational, employment, legal, mental health and family
problems, medical, Substance Use Disorder, HIV or other communicable diseases, pregnancy and
prenatal care, and social services are made available to Patients who demonstrate a need for such
services. Support services may be provided either directly or by appropriate referral. Support
services recommended and utilized shall be documented in the Patient record.
2. When appropriate, the Opioid Treatment Program shall link the Patient with an educational
program, and vocational employment services. Deviations from compliance with these outcomes shall
be documented in the Patient’s record.
3. The Opioid Treatment Program shall establish and utilize formal linkages with community-
based treatment services, through an established set of procedures for coordinating care with
Physicians or other health or behavioral care providers when appropriate.
4. The Opioid Treatment Program shall establish linkages with the criminal justice system to
encourage continuous treatment of individuals incarcerated or on probation and parole.
C. Services to Pregnant Patients in an Opioid Treatment Program (II).
1. The Facility shall make reasonable effort to ensure that pregnant Patients receive prenatal care
by a Physician and that the Physician is notified of the Patient’s participation in the Opioid
Treatment Program when the Facility becomes aware of the pregnancy.
2. The Opioid Treatment Program shall provide, through in-house services or referral, and
document in the Individual Plan of Care, appropriate services and interventions for the pregnant
Patient to include:
a. Physician consultation at least monthly;
b. Nutrition counseling; and
c. Parenting training to include newborn care, health and safety, parent/infant interaction, and
bonding.
3. The Facility shall maintain signed documentation of a Patient’s acknowledgement of refusal of
prenatal care.
4. Opioid Treatment Program FDA-approved Medication for opioid treatment dosage levels shall
be maintained at an appropriate level for pregnant Patients as determined by the Opioid Treatment
Program Physician and documented in the Patient’s record. (I)
5. When a pregnant Patient chooses to discontinue participation in the Opioid Treatment
Program, the program Physician, in coordination with the attending obstetrician, shall supervise the
termination process.
904. Substance Use Testing for Opioid Treatment Programs (II).
A. Substance use testing shall be used as a clinical tool for the purposes of diagnosis and in the
development of Individual Plans of Care.
B. Substance use testing for the presence of Opioid Treatment Program Medication, benzodiaze-
pines, cocaine, opiates, marijuana, amphetamines, and barbiturates, as well as other substances, when
clinically indicated by the Opioid Treatment Program Physician, shall be conducted at a frequency as
determined by the Opioid Treatment Program.
C. Results of substance use testing shall be addressed by the primary Counselor with the Patient, in
order to intervene in Controlled Substance use behavior.
D. The Opioid Treatment Program shall establish and implement written testing procedures,
including random collection of substance testing samples, to effectively minimize the possibility of
falsification of the sample, to include security measures for prevention of tampering.
E. Patients granted take home dosages shall undergo random substance use testing on a monthly
basis. For Patients whose substance use testing reports indicate positive results for any illicit substances,
non prescription Medications, or a negative result of Opioid Treatment Program Medication, the
frequency for substance use testing shall be determined by the Opioid Treatment Program Physician or
other Authorized Healthcare Provider. Documentation of the rationale for the frequency shall be
documented in the Patient’s medical record.
F. Only those laboratories certified in accordance with the federal Clinical Laboratories Improve-
ment Amendments shall be utilized by the Opioid Treatment Program for urinalysis.
905. Orientation for Patients Admitted to an Opioid Treatment Program.
Patient orientation shall be accomplished within seven (7) calendar days of admission and documented
in the Patient record. The orientation shall include:
A. Opioid Treatment Program guidelines, rules, and regulations;
B. Confidentiality;
C. Substance use testing procedure;
D. Administering Opioid Treatment Program Medication;
E. Signs and symptoms of an overdose and when to seek emergency assistance;
F. Discharge procedures;
G. Treatment phases;
H. HIV/AIDS information and education;
I. Patient rights (See Section 1000);
J. The nature of Substance Use Disorders and recovery including misunderstandings regarding
methadone or other opioid treatment Medication; and
K. For pregnant Patients, risk to the unborn child.
906. Transportation.
Residential Facilities shall provide or assist in securing local transportation for Patients for emergent
or non-emergent health reasons to health care providers such as, but not limited to, Physicians,
dentists, physical therapists, or for treatment at renal dialysis clinics.
907. Safety Precautions and Restraints (I).
A. Periodic or continuous mechanical, physical, or chemical restraints during routine care of a
Patient shall not be used, nor shall Patients be restrained for Staff convenience or as a substitute for
care or services. However, in cases of extreme emergencies when a Patient is a danger to him or herself
or others, mechanical and/or physical restraints may be used as ordered by a Physician or other
Authorized Healthcare Provider, and until appropriate medical care can be secured. Only those
devices specifically designed as restraints may be used.
B. Emergency restraint orders shall specify the reason for the use of the restraint, the type of
restraint to be used, the maximum time the restraint may be used, and instructions for observing the
Patient while restrained, if different from the Facility’s written procedures. Patients certified by a
Physician or other Authorized Healthcare Provider as requiring restraint for more than twenty-four
(24) hours shall be transferred to an appropriate Facility.
C. During emergency restraint, Patients shall be monitored at least every fifteen (15) minutes and
provided with an opportunity for motion and exercise at least every thirty (30) minutes. Prescribed
Medications and treatments shall be administered as ordered, and Patients shall be offered nourish-
ment and fluids and given bathroom privileges.
D. The use of mechanical restraints shall be documented in the Patient’s record, and shall include
the date and time implemented, the length of time restrained, observations while Patient is restrained.
908. Services for Minors (II).
A. In Residential Facilities, Minors shall be housed separately from adults except in Facilities
providing services for Parents with children.
B. In those instances where Minors are served, the Facility shall ensure that the special needs of
these Patients are addressed, including, but not limited to, education-related considerations.
C. The Facility shall ensure treatment and counseling are conducted to meet the physical, mental,
and emotional developmental needs of the Minor.
D. The Facility shall refer Minors who require special medical needs to a Physician who has clinical
experience with Minors and dependency. The Facility shall monitor Minors for treatment reactions
that may be developmentally detrimental. A plan shall be in place in the event that special medical care
is required.
909. Referral Services.
A. Referrals for care and/or services shall not be made to unlicensed Facilities if such Facilities are
required to be licensed. (II)
B. The Facility shall provide information regarding appropriate self-help groups to Patients and
encourage their participation in such activities, and document the information was provided in the
Patient’s record.
C. The facility shall maintain documentation of the rationale for the denial of admission and
referral for services offered to the Patient as applicable.
D. A community resource file shall be developed, maintained, and used for proper Patient referral
and placement. The file shall include a listing of services, fees, hours of operation, and contact person
as well as material to be provided to the Patient. The Facility shall provide the Patient with information
and offer referral for community resources such as transportation, hospital emergency services, and
ambulance services.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 900 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 1000. PATIENT RIGHTS AND ASSURANCES
1001. Informed Consent (II).
A. Upon admission, there shall be a written, signed, and dated informed consent between the
Patient and the Facility. The informed consent shall include at least the following:
1. An explanation of the specific care, services, and/or equipment provided by the Facility, such
as, administration of Medication, provision of special diet as necessary, assistance with bathing,
toileting, feeding, dressing, and mobility;
2. Discharge and transfer provisions to include the conditions under which the Patient may be
Discharged, and the agreement terminated, and the disposition of personal belongings; and
3. Documentation of the explanation of the Patient’s rights (see Section 1002) and the grievance
procedure.
4. Each person enrolling in an Opioid Treatment Program shall be notified of the autopsy
provision in South Carolina Code Section 44–53–750 as a part of such person’s informed consent.
B. The provision of care and services to Patients shall be guided by the recognition of and respect
for cultural differences to ensure reasonable accommodations shall be made for Patients with regard to
differences, such as, but not limited to, religious practice and dietary preferences.
1002. Patient Rights (II).
A. Patient rights shall be guaranteed and prominently displayed in a public area. Documentation of
the explanation of the Patient’s Bill of Rights shall be maintained in the Patient’s medical record. The
Patient rights shall include:
1. The opportunity to participate in the Individual Plan of Care;
2. Informed consent for treatment;
3. Grievance and/or complaint procedures, including the address and phone number of the
Department, and a provision prohibiting retaliation should the grievance right be exercised;
4. Confidentiality of Patient records;
5. Respect for the Patient’s property (Residential Facilities Only);
6. Freedom from Abuse, Neglect, and Exploitation; (I)
7. Privacy in visits unless contraindicated in the recovery and treatment process or as ordered by
a Physician or other Authorized Healthcare Provider;
8. Privacy during treatment and while receiving personal care; and
9. Respect and dignity in receiving care, treatment, and services.
B. For Facilities providing Residential Services, the Patients shall be assured freedom of movement.
Patients shall not be locked in or out of their rooms or any common usage areas, in the Facility, or in
or out of the Facility building. (I)
C. Care and services and items provided by the Facility, the charge, and those services that are the
responsibility of the Patient shall be delineated in writing and the Patient shall be made aware of such
charges and services as verified by his or her signature.
D. The Facility shall comply with all current federal, state, and local laws and regulations related to
discrimination, e.g., Title VII, Section 601 of the Civil Rights Act of 1964, ADA, and ensure that there
is no discrimination with regard to source of payment in the recruitment, location of Patient,
acceptance or provision of goods and services to Patients or potential Patients, provided that payment
offered is not less than the cost of providing services.
E. In Residential Facilities, no care and/or treatment and/or services shall be provided to individu-
als who are not Patients of the Facility, except those services provided to family members as part of the
Patient’s recovery plan.
1003. Discharge and Transfer.
A. Unless a Patient is under court order or detained subject to a pending judicial process, a Patient
may be transferred or Discharged only for medical reasons, the welfare of the Patient, the welfare of
other Patients of the Facility, lack of progress or participation in treatment, or successful completion of
the program. He or she shall be given written notice of Discharge except when the health, safety, or
well-being of other Patients of the Facility would be endangered.
B. When a Patient is transferred from one Facility to another, a transfer summary, to include
copies of relevant documents, shall be forwarded to the receiving Facility within a time-period as
determined by the Facility but not to exceed seventy-two (72) hours from transfer. The Facility shall
ensure that Medication, personal possessions and funds of the Patient are forwarded to the receiving
Facility and/or site in a manner that ensures continuity of care and/or treatment and/or services and
maximum convenience to the Patient.
C. A Patient transferring from another Opioid Treatment Program shall have a Physical Examina-
tion upon admission and have his or her dose determined by a Physician prior to receiving the first
dosage.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020; SCSR 44–6 Doc. No. 4954, eff June 26, 2020
(errata). Transferred from 61–93 § 1000 by SCSR 49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 1100. PATIENT PHYSICAL EXAMINATION
A. Residential Facilities. A Physical Examination shall be completed by a Physician or other
Authorized Healthcare Provider for Patients within thirty (30) calendar days prior to admission or two
(2) business days of admission for Patients. Physical Examinations conducted by Physicians or other
Authorized Healthcare Providers licensed in other states are permitted for new admissions under the
condition that the Patient undergoes a second Physical Examination by a South Carolina licensed
Physician or other Authorized Healthcare Provider within thirty (30) calendar days of admission to the
Facility. The Physical Examination shall address:
1. The appropriateness of level of services;
2. Identification of special conditions and/or care required;
3. A tuberculin skin test, as described in Section 1702, unless there is a previously documented
positive reaction;
4. If a Patient or potential Patient has a communicable disease, the Facility shall follow the
recommendations made by a Physician or other Authorized Healthcare Provider in order to:
a. Ensure that the Facility has the capability of providing adequate care and preventing the
spread of that condition, and that Staff and Volunteers are adequately trained; or
b. Transfer the Patient to an appropriate Facility, if necessary; and
5. A substance use test. Following the test, the Physician or Authroized Healthcare Provider shall
determine the frequency of subsequent testing based on the Patient’s clinical presentation.
B. In Facilities providing services for parents with children, there shall be a report of an
examination for each child by a Physician or other Authorized Healthcare Provider attesting to the
health status and special care needs that may impact the child, his/ or her parent, and/or others within
the Facility. The examination shall be conducted not earlier than thirty (30) calendar days prior to the
parent’s admission or no later than forty-eight (48) hours after admission.
C. Opioid Treatment Program.
1. Physical Examination. A Physical Examination conducted by the Opioid Treatment Program
Physician or other Authorized Healthcare Provider shall be completed within seventy-two (72) hours
prior to the first dose of Opioid Treatment Program Medication and shall address the following at a
minimum: (I)
a. Evidence of communicable or Infectious disease;
b. Pulmonary, liver, renal, and cardiac abnormalities;
c. Neurological issues;
d. Vital signs;
e. Evidence of clinical signs of dependency; and
f. Examination of head, ears, eyes, nose, throat, thyroid, chest (including heart, lungs and
breast), abdomen, extremities, and skin.
2. Medical Laboratory Analysis. A medical laboratory analysis shall be conducted within seven (7)
calendar days of admission and shall include:
a. Serological test for Infectious disease;
b. Initial substance use testing for Controlled Substance profile;
c. Liver profile; and
d. If indicated, an electrocardiogram, chest x-ray, and/or a biological pregnancy test.
3. In the event the medical staff are unable to obtain an adequate blood draw for the medical
laboratory analysis on the first attempt, the Facility shall reattempt within the seven (7) days of
admission. After three (3) documented attempts within the seven (7) days of admission, the Opioid
Treatment Program Physician or other Authorized Healthcare Provider may waive the blood testing
requirements. The Physician’s decision shall be documented in the Patient’s medical record. The
Facility shall follow its policies and procedures related to infection control if the Physician waives the
blood testing requirement.
D. In the event that a Patient transfers from one Residential Facility to another, an additional
admission Physical Examination and/or tuberculin skin test shall not be necessary, provided the
Physical was conducted not earlier than twelve (12) months prior to the admission of the Patient, and
the Physical meets all other requirements specified in Section 1100.A.1, unless the receiving Facility has
an indication that the health status of the Patient has changed significantly. In such instances of
transfer, issues of appropriateness of level of treatment placement shall be addressed in the Patient
record.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 1100 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 1200. MEDICATION MANAGEMENT
1201. General (I).
A. Medications, including Controlled Substances, medical supplies, and those items necessary for
the rendering of first aid shall be properly managed in accordance with local, state, and federal law
and regulations, which includes the securing, storing, and administering, dispensing, and delivering of
medications, medical supplies, and biologicals, their disposal when discontinued or outdated, and their
disposition at Discharge, death, or transfer of a Patient. All Facilities that manage Medication of
Patients shall comply with this section.
B. Applicable reference materials published within the previous three (3) years shall be available at
the Facility in order to provide Staff and/or Volunteers with adequate information concerning
Medications.
1202. Medication Orders (I).
A. Medication, including oxygen, shall be administered and delivered to Patients only upon orders
of a Physician or other Authorized Healthcare Provider. Medications accompanying Patients at
admission may be administered and/or delivered to Patients, provided the Medication is in the original
container and the order/authorization is subsequently obtained as a part of the admission Physical
Examination. If there are concerns regarding whether or not such Medications should be administered
and/or delivered due to the condition or state of the Medication, e.g., old, expired, makeshift labels, or
the condition or state of health of the newly-admitted individual, Staff and Volunteers shall consult
with or make arrangements to have the Patient examined by a Physician or other Authorized
Healthcare Provider, or at the local hospital emergency room prior to administering or delivering any
Medications.
B. All orders (including verbal orders) shall be signed and dated by a Physician or other Authorized
Healthcare Provider within a time-period as designated by the Facility, but no later than seventy-two
(72) hours after the order is given.
C. In an Opioid Treatment Program, all orders shall be documented, signed, and dated by the
Opioid Treatment Program Physician. The Opioid Treatment Program Physician shall determine the
initial and subsequent dosage and schedule, and prescribe such dose and schedule to include changes
by verbal or written order to the pharmacist and Licensed Nurse. However, the verbal order shall be
documented, signed, and dated by the Opioid Treatment Program Physician within seventy-two (72)
hours.
D. Orders for Controlled Substances shall be authenticated by the prescribing Physician or
designee.
E. Medications and medical supplies ordered for a specific Patient shall not be administered and/or
delivered to any other Patient.
1203. Administering Medication (I).
A. Doses of Medication shall be administered by the same Licensed Nurse who prepared them for
administration. Preparation shall occur no earlier than one (1) hour prior to administering. Prepara-
tion of doses for more than one (1) scheduled administration shall not be permitted. Each Medication
dose administered shall be recorded on the Patient’s Medication administration record (‘‘MAR’’) as it is
administered. Should an ordered dose of Medication not be administered, an explanation as to the
reason shall be recorded on the MAR. The recording of Medication administration shall include: the
medication name, dosage, mode of administration, date, time, and the signature of the individual
administering or supervising the taking of the Medication. Initials in lieu of signatures are acceptable
provided such initials can be readily identified on the MAR. If the ordered dosage is to be given on a
varying schedule, for example, ‘‘take two tablets the first day and one tablet every other day by mouth
with noon meal,’’ the number of tablets shall also be recorded.
B. When a Physician or other Authorized Healthcare Provider changes the dosage of a Medication,
a new entry reflecting the change shall be documented in the Medication administration record
(‘‘MAR’’). No dose shall be administered until the Patient’s identity has been verified and the dosage
compared with the currently ordered and documented dosage level. Ingestion shall be observed and
verified by the person authorized to administer the Medication.
C. Opioid Treatment Program Only:
1. The Facility shall not administer a Patient’s initial dose of Opioid Treatment Program
Medication until the program Physician or other Authorized Healthcare Provider has determined
that all admission criteria have been met, to include a completed Physical Examination by the
program Physician or other Authorized Healthcare Provider and confirmation of current Medication
regimen being taken by the applicant.
2. The initial dose of methadone shall not exceed thirty (30) milligrams and the initial total daily
dose for the first day shall not exceed forty (40) milligrams unless the Opioid Treatment Program
Physician or other Authorized Healthcare Provider justifies in the Patient record that forty (40)
milligrams did not suppress the abstinence symptoms after three (3) hours of observation following
the initial dose. There shall be written justification in the Patient record, signed and dated by the
Opioid Treatment Program Physician or other Authorized Healthcare Provider, for doses in excess
of one hundred (100) milligrams of methadone per day after the first day.
3. A Patient’s scheduled dose may be temporarily delayed if necessary, e.g., to obtain a urine
sample or for Counselor consultation. The dose shall not be withheld, however, for failure to comply
with the Opioid Treatment Program rules or procedures unless the decision is made to terminate
the Patient’s participation in the Opioid Treatment Program. A dose may be withheld only when the
Opioid Treatment Program Physician or other Authorized Healthcare Provider determines that such
action is medically indicated.
4. When the Opioid Treatment Program Physician prescribes Controlled Substances other than
Opioid Treatment Program Medications, such prescriptions shall not be administered to any Patient
unless the Opioid Treatment Program Physician or other Authorized Healthcare Provider first
examines the Patient and assesses his or her potential for misuse of such Medications.
D. Self-administration of Medications shall be allowed only on the specific written orders of a
Physician or other Authorized Healthcare Provider. An appropriate Staff member delivering the
Medication shall document the delivery. Such documentation shall include the date, time, and the
signature of the individual delivering the Medication.
E. When Patients who cannot Self-Administer Medications leave the Facility for an extended time,
the proper amount of Medications, placed into a prescription vial or bottle, along with dosage, mode,
date, and time of administration, shall be given to a responsible person who will be in charge of the
Patient during his or her absence from the Facility and properly documented in the Medication
administration record. If there is no designated responsible party for the Patient, then the attending
Physician or other Authorized Healthcare Provider shall be contacted for proper instructions.
F. The Medications prescribed for a Patient shall be protected from use by other Patients, visitors,
and Staff and Volunteers. For those Patients who have been authorized by a Physician or other
Authorized Healthcare Provider to Self-Administer Medications, such Medications (nitroglycerin,
rescue inhalers, epinephrine auto-injectors) may be kept on the Patient’s person, i.e., a pocketbook,
pocket, or any other method that would enable the Patient to control the items.
1204. Pharmacy Services (I).
A. Any pharmacy within the Facility shall be provided by or under the direction of a licensed
pharmacist in accordance with accepted professional principles and appropriate federal, state, and local
laws and regulations.
B. Facilities that maintain stocks of Medications and biologicals for Patient use within the Facility
shall obtain and maintain from the South Carolina Board of Pharmacy a valid, current, non-dispensing
drug outlet permit that is displayed in a conspicuous location in the Facility.
C. Labeling of Medications dispensed to Patients shall be in compliance with local, state, and
federal laws and regulations applicable to retail pharmacies.
1205. Medication Containers (I).
A. Medications for Patients shall be obtained from a permitted pharmacy or Authorized Healthcare
Provider as allowed by law on an individual prescription basis. These Medications shall bear a label
affixed to the container that reflects at least the following: name of pharmacy, name of Patient, name of
the prescribing Physician or other Authorized Healthcare Provider, date and prescription number,
directions for use, and the name and dosage unit of the Medication. The label shall be brought into
accord with the directions of the Physician or other Authorized Healthcare Provider each time the
prescription is refilled. Medication containers having soiled, damaged, incomplete, illegible, or make-
shift labels shall be returned to the pharmacy for re-labeling or disposal.
B. Medications for each Patient shall be kept in the original container(s) including unit dose
systems; there shall be no transferring between containers or opening blister packs to remove
Medications for destruction or adding new Medications for administration, except under the direction
of a pharmacist. In addition, for those Facilities that utilize the unit dose system or multi-dose system,
an on-site review of the Medication program by a pharmacist shall be conducted on at least a quarterly
basis to ensure the program has been properly implemented and maintained. For changes in dosage,
the new packaging shall be available in the Facility no later than the next administration time
subsequent to the order. This shall be documented and signed by the pharmacist.
C. Medications for Patients shall be obtained from a permitted pharmacy or prescriber on an
individual prescription basis. These Medications shall bear a label affixed to the container that reflects
at least the following: name of pharmacy, name of Patient, name of the prescribing Physician or
dentist, date and prescription number, directions for use, and the name and dosage unit of the
Medication.
D. When a Physician or other legally Authorized Healthcare Provider changes the dosage of a
Medication, such information shall be documented in the Medication administration record and a label
that does not obscure the original label shall be attached to the container that states, ‘‘Directions
changed; refer to MAR and Physician or other Authorized Healthcare Provider orders for current
administration instructions.’’
1206. Medication Storage (I).
A. Medications may be stored in a separate locked box within a refrigerator at or near the
Medication storage area, either behind a locked door or the refrigerator shall be locked.
B. Controlled Substances and ethyl alcohol shall be stored in accordance with applicable state and
federal laws. A record of the stock and distribution of all Controlled Substances shall be maintained in
such a manner that the disposition of any particular item may be readily traced.
C. Medications shall be stored:
1. Separately from poisonous Controlled Substances or body fluids;
2. In a manner which provides for separation between topical and oral Medications, and which
provides for separation of each individual Patient’s Medication.
D. Stock Medications
1. Unless the Facility has a permitted pharmacy, stocks of Legend Medications shall not be stored
except those specifically prescribed for individual Patients.
2. Non-legend Medications may be retained and labeled as stock in the Facility for administration
as ordered by a Physician or other Authorized Healthcare Provider.
3. Stocks of naloxone may be stored for emergency overdose crises, with or without specific
prescription for individual Patients.
4. If stock non-Patient specific Controlled Substances are to be used, a Controlled Substances
registration from the Department’s Bureau of Drug Control and a Controlled Substances registra-
tion from the federal Drug Enforcement Administration shall be obtained. The registrations shall be
displayed in a conspicuous location within the Facility.
E. No Medications may be left in a Patient’s room unless the Facility provides an individual
cabinet/compartment that is kept locked in the room of each Patient who has been authorized to Self-
Administer in writing by a Physician, or other Authorized Healthcare Provider. In lieu of a locked
cabinet or compartment, a room that can be locked and is licensed for a capacity of one (1) Patient is
acceptable provided the Medications are not accessible by unauthorized persons, the room is kept
locked when the Patient is not in the room, the Medications are not Controlled Substances, and all
other requirements of this section are met.
F. The Medications prescribed for a Patient shall be protected from use by other Patients, visitors
and Staff and Volunteers. For those Patients who have been authorized by a Physician or other
Authorized Healthcare Provider to self-administer Medications, such Medications may be kept on the
Patient’s person, i.e., a pocketbook, pocket, or any other method that would enable the Patient to
control the items.
G. During nighttime hours in semi-private rooms, only Medications that a Physician or other
Authorized Healthcare Provider has ordered in writing for emergency/immediate use, e.g., nitroglyce-
rin, rescue inhalers, or epinephrine auto-injectors may be kept unlocked in or upon a cabinet or
bedside table, and only when the Patient to whom that Medication belongs is present in the Patient
room.
1207. Disposition of Medications (I).
A. The Facility shall release Medications to the Patient upon Discharge, unless specifically prohibit-
ed by the ordering Physician or Authorized Healthcare Provider.
B. Patient’s Medications shall be destroyed by the Facility Administrator or his or her designee or
returned to dispensing pharmacy when:
1. Medication has deteriorated or exceeded its safe shelf-life; and
2. Unused portions remain due to death, Discharge, or discontinuance of the Medications.
Medications that have been discontinued by order may be stored for a period not to exceed thirty
(30) calendar days provided they are stored separately from current Medications.
C. The destruction of Medication shall occur within five (5) days of the above-mentioned circum-
stances, be witnessed by the Administrator or his or her designee, and the mode of destruction
indicated.
D. The destruction of controlled substances Medications shall be accomplished only by the
Administrator or his or her designee on-site and witnessed by a Licensed Nurse or pharmacist, or by
returning them to the dispensing pharmacy and obtaining a receipt from the pharmacy.
1208. Opioid Treatment Program Take-home Medication (II).
A. Opioid Treatment Program Medication, including guest and take-home doses, shall be adminis-
tered to Patients in single doses. Take-home bottles shall be labeled in accordance with federal and
state law and regulations and shall contain necessary cautionary statements; caps shall be childproof.
B. Take-home Opioid Treatment Program Medication may be given to Patients who demonstrate a
need for a more flexible schedule in order to enhance and continue the rehabilitative process.
However, since Opioid Treatment Program Medication is an opioid subject to misuse if not managed
properly, precautions shall be taken to prevent its potential misuse. The Opioid Treatment Program
Physician shall ensure that take-home Medication is given to those Patients who meet the following
criteria for eligibility:
1. Adherence to Opioid Treatment Program rules, regulations, and policies;
2. Length of time in the Opioid Treatment Program and level of maintenance treatment;
3. Presence of Opioid Treatment Program Medication in substance use testing;
4. Potential complications from concurrent health problems;
5. Lengthy travel distance to the Facility; and
6. Progress in maintaining a stable lifestyle as evidenced by:
a. Absence of misuse of opioids and non-opioids;
b. Absence of alcohol misuse, or determination that the using alcohol and is in treatment for
the alcohol misuse problem;
c. Regularity of attendance at the Opioid Treatment Program, to include required counseling
sessions;
d. Absence of serious behavior problems, including loitering at the Opioid Treatment Pro-
gram;
e. Absence of known recent criminal activity;
f. Employment, school attendance, or other appropriate activity; and
g. Assurance that take-home Medication can be securely transported and stored by the Patient
for his or her use only.
C. The decision to provide take-home Medication to Opioid Treatment Program Patients and the
amount provided shall be based upon and determined by the reasonable clinical judgment of the
Opioid Treatment Program Physician and appropriately documented and recorded in the Patient’s file
prior to the initiation of the take-home dose. The Opioid Treatment Program Physician shall
document compliance by the Patient with all of the aforementioned requirements prior to providing
the first take-home dose. (I)
D. The Patient’s take-home status shall be reviewed and documented at least on a quarterly basis by
the primary Counselor.
E. If a Patient, due to special circumstances, such as illness, personal or family crisis, travel, or
other hardship, is unable to conform to the applicable treatment schedule, he or she may be permitted
to receive up to a two (2)-week supply of Opioid Treatment Program Medication, based on the clinical
judgment of the Opioid Treatment Program Physician. The justification for permitting the adjusted
schedule shall be recorded in the Patient’s record by the Opioid Treatment Program Physician.
F. One-time or temporary (usually not to exceed three (3) days) take-home Medication shall be
approved by the Facility for family or medical emergencies or other exceptional circumstances.
G. A Patient transferring from another Opioid Treatment Program or readmitted after having left
the Opioid Treatment Program voluntarily and who has complied with Facility rules and program
policies and procedures may be granted an initial take-home schedule that is no greater than that
allowed at the time of transfer or voluntary Discharge provided all criteria other than length of
treatment are met.
H. A Patient discharged from another Opioid Treatment Program shall only be initially granted
take-home privileges from the new admitting Opioid Treatment Program provided the requirements
of Section 1209 are met.
I. Take-home Medication shall be labeled with the name of the Opioid Treatment Program,
address, telephone number, and packaged in conformance with state and federal regulations.
J. A diversion control plan shall be established to assure quality care while preventing the diversion
of Opioid Treatment Program Medication from treatment to illicit use. The plan shall include:
1. Clinical and administrative continuous monitoring;
2. Problem identification, correction and prevention;
3. Accountability to the Patient and community; and
4. Opioid Treatment Program Medication usage and amount accountability.
1209. Opioid Treatment Program Guest-Dosing (II).
A. When a Patient is separated from his or her Opioid Treatment Program for an extended period,
and the Patient is in the vicinity of another Licensed Opioid Treatment Program, guest-dosing may
occur provided there is: (I)
1. Authorization in writing from the sending Opioid Treatment Program Physician or other
Authorized Healthcare Provider; and
2. Information from the sending Opioid Treatment Program to include at least the following:
Patient name, identifying information, means of identity verification, dates of guest-dosing, amount
of each day’s dose, number of take-home doses (if any), urinalysis history, and any other information
requested by the authorizing treatment Opioid Treatment Program.
B. Records of guest-dosing shall be maintained at the Opioid Treatment Program providing the
guest-dosing.
C. Guest-dose status for a Patient shall not exceed twenty-eight (28) days unless there are special
circumstances, and an extension of time is agreed upon by the two (2) Opioid Treatment Programs
involved.
D. A Facility desiring to administer guest dosing for Patients from neighboring states in the event
of a natural disaster or emergency shall:
1. Request that the Department concur that an emergency situation exists by contacting the
Department;
2. Administer the guest-dosing only upon written orders from the Facility’s Opioid Treatment
Program physician; and
3. Maintain documentation of the physician’s rationale for the dosing protocol and information
utilized to make the decision.
1210. Security of Medications (I).
A. The areas where Opioid Treatment Program stock Medications are maintained or administered
shall be secured. Access to Controlled Substances, which include Opioid Treatment Program Medi-
cations, shall be limited to persons licensed or registered to order, administer, or dispense those
Medications.
B. Immediately after administering, the remaining contents of the containers shall be purged to
prevent the accumulation of residual Opioid Treatment Program Medications. The Opioid Treatment
Program shall ensure that take-home Medications bottles are returned to the Opioid Treatment
Program. All used containers, as well as take-home bottles given to Patients, shall be made inaccessible
to unauthorized individuals. Used containers shall be disposed of by the Opioid Treatment Program.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 1200 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 1300. MEAL SERVICE
1301. General (II).
A. All Facilities that prepare food on-site shall be approved by the Department, and shall be
regulated, inspected, and graded pursuant to R.61–25, Retail Food Establishments. Facilities preparing
food on-site, licensed for sixteen (16) beds or more subsequent to the promulgation of this regulation
shall have commercial kitchens. Existing Facilities with sixteen (16) licensed beds or more may continue
to operate with equipment currently in use; however, only commercial kitchen equipment shall be
used when replacements are necessary. Those Facilities with fifteen (15) beds or less shall be regulated
pursuant to R.61–25 with certain exceptions in regard to equipment (may utilize domestic kitchen
equipment).
B. When meals are catered to a Facility, such meals shall be obtained from a food service
establishment permitted by the Department, pursuant to R.61–25 and there shall be a written executed
contract with the food service establishment on file in the Facility.
C. All food to be served to Patients shall be transported, received, stored, and handled in
accordance with R.61–25. Washing and sanitation of all food contact and non-food contact surfaces,
equipment, and utensils shall meet the standards required by R.61–25. A handwash lavatory shall be
provided in the food service area equipped with liquid soap and a hand drying provision. Hand
sanitizers shall not be used in lieu of liquid soap.
D. If food is prepared at a central kitchen and delivered to separate Facilities or separate buildings
and/or floors of the same Facility, provisions shall be made and approved by the Department for
proper maintenance of food temperatures and a sanitary mode of transportation.
E. Food shall be prepared by methods that conserve the nutritive value, flavor, and appearance.
The food shall be palatable, properly prepared, and sufficient in quantity and quality to meet the daily
nutritional needs of the Patients in accordance with written dietary policies and procedures. Efforts
shall be made to accommodate the religious, cultural, and ethnic preferences of each individual Patient
and consider variations of eating habits, unless the orders of a Physician or other Authorized
Healthcare Provider contraindicate.
1302. Food and Food Storage (II).
Residential Facilities shall maintain at least a one (1)-week supply of staple foods and a two (2)-day
supply of perishable foods on the premises. Supplies shall be appropriate to meet the requirements of
the menu and special diets.
1303. Meals and Services.
A. Residential Facilities shall serve a minimum of three (3) nutritionally-adequate meals in each
twenty-four (24)-hour period unless otherwise directed by the Patient’s Physician or other Authorized
Healthcare Provider. Not more than fourteen (14) hours shall elapse between the serving of the
evening meal and breakfast the following day. (II)
B. Specific times for serving meals shall be established, documented on a posted menu, and
followed.
C. Suitable food and snacks shall be available and offered between meals at no additional cost to the
Patients. (II)
1304. Meal Service Personnel for Residential Facilities (II).
A. The health, disease control, and cleanliness of all those engaged in food preparation and serving
shall be in accordance with R.61–25.
B. Dietary services shall be organized with established lines of accountability and clearly defined job
assignments for those engaged in food preparation and serving. There shall be trained Staff and/or
Volunteers to supervise the preparation and serving of the proper diet to the Patients. Patients may
engage in food preparation in accordance with Facility guidelines; however, trained Staff and/or
Volunteers shall supervise.
1305. Menus.
A. Menus shall be planned and written at a minimum of one (1) week in advance and dated as
served. The current week’s menu, including routine and special diets and any substitutions or changes
made, shall be readily available or posted in one (1) or more conspicuous places in a public area. All
substitutions made on the master menu shall be recorded in writing.
B. If the Facility accepts Patients in need of medically-prescribed special diets, the menus for such
diets shall be planned by a professionally qualified Dietitian, or shall be reviewed and approved by a
Physician or other Authorized Healthcare Provider. The Facility shall maintain documentation that
each of these menus has been planned by a Dietitian, a Physician, or other Authorized Healthcare
Provider. At a minimum, documentation for each Patient’s special diet menu shall include the
signature of the Dietitian, the Physician, or other Authorized Healthcare Provider, his or her title, and
the date he or she signed the menu.
C. Records of menus as served shall be maintained for at least thirty (30) days.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 1300 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 1400. EMERGENCY PROCEDURES AND DISASTER PREPAREDNESS
1401. Disaster Preparedness (II).
A. All Residential Facilities shall develop, by contact and consultation with their county emergency
preparedness agency, a written plan for actions to be taken in the event of a disaster and implement
the written plan for actions at the time of need. Prior to initial licensing of a Facility by the
Department, the completed plan shall be submitted to the Department for review. At the time of each
License renewal, a completed form prescribed and furnished by the Department addressing specific
components of the plan shall be included with each application submitted to the Department. All Staff
and Volunteers shall be made familiar with this plan and instructed as to any required actions. A copy
of the plan shall be available for Inspection by the Patient and/or responsible party and the
Department upon request. The plan shall be reviewed and updated Annually, and as appropriate. The
Facility shall conduct and document a rehearsal of the emergency and disaster evacuation plan at least
Annually and shall not require Patient participation.
B. The disaster plan for Residential Facilities shall include, but not be limited to:
1. A sheltering plan to include:
a. The licensed bed capacity and average occupancy rate;
b. Name, address, and phone number of the sheltering facility(ies) to which the Patients will be
relocated during a disaster; and
c. A letter of agreement signed by an authorized representative of each sheltering facility that
shall include: the number of relocated Patients that can be accommodated; sleeping, feeding, and
medication plans for the relocated Patients; and provisions for accommodating relocated staff. The
letter shall be updated annually with the sheltering facility and whenever significant changes
occur. For those facilities located in Beaufort, Berkeley, Charleston, Colleton, Dorchester, Horry,
Jasper, and Georgetown counties, at least one (1) sheltering facility must be located in a county
other than these counties.
2. A transportation plan to include agreements with entities for relocating Patients that address-
es:
a. The number and type of vehicles required;
b. How and when the vehicles are to be obtained;
c. Who (by name or organization) will provide drivers;
d. Procedures for providing appropriate medical support during relocation;
e. The estimated time to accomplish the relocation; and
f. The primary and secondary routes to be taken to the sheltering facility.
3. A staffing plan for the relocated Patients to include:
a. How care will be provided to the relocated Patients including the number and type of Staff;
b. Plans for relocating Staff or assuring transportation to the sheltering facility; and
c. Co-signed statement by an authorized representative of the sheltering facility if staffing will
be provided by the sheltering facility.
4. A written, signed, and dated statement from the county emergency preparedness agency
verifying the Facility’s plan was developed and reviewed through contact and consultation with the
county emergency preparedness agency.
C. During any emergent event, the Facility shall provide data, Facility and evacuation status, and
other requested information as determined by the Department, and at a frequency as determined by
the Department.
D. Evacuation is a temporary measure in order to evacuate Patients from potentially hazardous
and/or harmful circumstances and shall not exceed seven (7) calendar days. In the event evacuated
Patients are unable to return to the Facility within seven (7) days due to damage to the Facility or its
components, the lack of electricity and/or water, or other similar reasons, the Facility shall endeavor to
assess each Patient’s current condition and identify each Patient’s current needs and preferences.
Based on the resources available, the Facility shall implement each Patient’s Discharge plan. For
Patients needing assistance or support following Discharge, the Facility shall coordinate the transfer of
the Patients to their responsible parties or to appropriately licensed Facilities capable of meeting the
Patients’ needs. Prior to the seventh (7th) day, if the Facility determines an extension of time is needed,
the Facility may request approval from the Department.
1402. Licensed Capacity During an Emergency (II).
A. In the event that the Facility temporarily provides shelter for evacuees who have been displaced
due to a disaster, then for the duration of that emergency, provided the health, safety, and well-being
of any Patient is not compromised, it is permissible to temporarily exceed the licensed capacity for the
Facility in order to accommodate these individuals.
B. A Facility desiring to temporarily admit Patients in excess of its licensed bed capacity due to an
emergency shall:
1. Request that the Department concur that an emergency situation exists by contacting the
Department;
2. Determine the maximum number of Patients to be temporarily admitted;
3. Establish an anticipated date for Discharge of the temporary Patients;
4. Outline how and where the temporary Patients will be housed; and
5. Contact the county emergency preparedness agency to advise them of additional Patients.
C. The Facility shall not require the Patients temporarily admitted during the emergency situation
to undergo tuberculin screening or submit to an admission history and physical examination.
D. The Facility shall notify the Department when the Patient census has returned to, or moves
below, normal bed capacity by Discharge or transfer to licensed beds.
E. If the event occurs after normal business hours, the Facility shall contact the Department
promptly during the next business day.
F. The Facility shall resolve in advance all other issues related to the temporary Patients (for
example, Staff, Physician orders, additional food, and handling of Medications) by memorandum of
agreements, internal policies and procedures, and emergency planning documents
1403. Emergency Call Numbers (II).
Emergency call data shall be posted in a conspicuous place and shall include at least the telephone
numbers of fire and police departments, an ambulance service, and the poison control center. Other
emergency call information shall be available, to include the names, addresses, and telephone numbers
of the Staff to be notified in case of emergency, and the Physician or other Authorized Healthcare
Provider on-call.
1404. Continuity of Essential Services (II).
There shall be a written plan to be implemented to assure the continuation of essential Patient
supportive services for such reasons as power outage, water shortage, or in the event of the absence
from work of any portion of the work force resulting from inclement weather or other causes.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 1400 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 1500. FIRE PREVENTION
1501. Arrangements for Fire Department Response (I).
A. Each Facility shall develop, in coordination with its supporting fire department and/or disaster
preparedness agency, suitable written plans for actions to be taken in the event of fire.
B. Facilities located outside of a service area or range of a public fire department shall arrange for
the nearest fire department to respond in case of fire by written agreement with that fire department.
A copy of the agreement shall be kept on file in the Facility and a copy shall be forwarded to the
Department. If the agreement is changed, a copy shall be forwarded to the Department.
1502. Fire Response Training (I).
A. Each Staff member and Volunteer shall receive training within twenty-four (24) hours of his or
her first day of employment in the Facility, and at least Annually thereafter, addressing at a minimum,
the following:
1. The Facility fire plan including evacuation routes and procedures;
2. Reporting a fire;
3. Use of the fire alarm system, if applicable;
4. Location and use of fire-fighting equipment;
5. Methods of fire containment; and
6. Specific responsibilities, tasks, or duties of each individual.
B. Documentation of the fire response training shall be signed and dated by both the individual
providing the training and the individual receiving the training, and maintained in the individual’s
Staff record.
1503. Fire Drills (I).
A. A plan for the evacuation of Patients, Staff members, and visitors, to include evacuation routes
and procedures, in case of fire or other emergencies, shall be established and posted in conspicuous
public areas throughout the Facility.
B. Patients shall be made familiar with the fire plan and evacuation plan upon admission. The
Facility shall maintain documentation of the review of the fire plan and evacuation plan with the
Patient in the Patient’s record.
C. All Patients capable of assisting in their own evacuation shall be trained in the proper actions to
take in the event of a fire.
D. For Residential Facilities only:
1. Unless otherwise mandated by statute or regulation, an unannounced fire drill shall be
conducted at least quarterly for all shifts. Each Staff member and Volunteer shall participate in a fire
drill at least once each year. Records of drills shall be maintained at the Facility, indicating the date,
time, shift, description, and evaluation of the drill, and the names of Staff and Volunteers and
number of Patients directly involved in responding to the drill.
2. All Patients at the time of the fire drill shall participate in the drill. In instances when a Patient
refuses to participate in a drill, efforts shall be made to encourage participation, e.g., counseling,
implementation of incentives rewarding patients for participation, specific Staff-to-Patient and
Volunteer-to-Patient assignments to promote Patient participation. Continued refusal may necessi-
tate implementation of the Discharge planning process to place the Patient in a setting more
appropriate to their needs and abilities.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 1500 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 1600. MAINTENANCE
1601. General (II).
A. The Facility shall keep all equipment and building components (for example, doors, windows,
lighting fixtures, plumbing fixtures) in good repair and operating condition. The Facility shall
document preventive maintenance. The Facility shall comply with the provisions of the codes officially
adopted by the South Carolina Building Codes Council and the South Carolina State Fire Marshal
applicable to the Facility. (II)
B. If applicable, a documented and implemented procedure shall be developed for calibrating
Medication-dispensing instruments consistent with manufacturer’s recommendations to ensure accu-
rate dosing and tracking.
1602. Preventive Maintenance of Emergency Equipment and Supplies (II).
Each Facility shall develop and implement a written preventive maintenance program for all fire
alarm, electrical, mechanical, plumbing, fire protection systems and for all equipment and supplies
including, but not limited to, all Patient monitoring equipment, isolated electrical systems, conductive
flooring, Patient grounding systems, and medical gas systems. Facilities shall check and/or test this
equipment at intervals ensuring proper operation and state of good repair. After repairs and/or
alterations to any equipment or system, the Facility shall thoroughly test the equipment or system for
proper operation before returning it to service. The Facility shall maintain records for each piece of
emergency equipment to indicate its history of testing and maintenance.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 1600 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 1700. INFECTION CONTROL AND ENVIRONMENT
1701. Staff Practices.
Staff practices shall promote conditions that prevent the spread of infectious, contagious, or
communicable diseases and provide for proper disposal of toxic and hazardous substances. These
preventive measures and/or practices shall be in compliance with applicable guidelines of Bloodborne
Pathogens Standard of the Occupational Safety and Health Act of 1970; the Centers for Disease
Control and Prevention and R.61–105, Infectious Waste Management; and other applicable federal,
state, and local laws and regulations.
1702. Tuberculosis Risk Assessment and Screening (I).
A. Tuberculosis Testing. The Facility may utilize either Tuberculin skin testing or Blood Assay for
Mycobacterium tuberculosis (‘‘BAMT’’) for detecting Myobacterium tuberculosis infection:
1. Tuberculin skin testing. A small dose (0.1 mil) of purified protein derivative (PPD) tuberculin
is injected just beneath the surface of the skin (by the intradermal Mantoux method), and the area is
examined for induration (hard, dense, raised area at the site of the TST administration) forty-eight
to seventy-two (48 to 72) hours after the injection (but positive reactions can still be measurable up to
a week after administering the TST). The size of the indurated area is measured with a millimeter
ruler and the reading is recorded in millimeters, including zero (0) millimeters to represent no
induration. Redness and/or erythema is insignificant and is not measured or recorded. Authorized
Healthcare Providers are permitted to perform tuberculin skin testing and symptom screening.
2. Blood Assay for Mycobacterium tuberculosis (‘‘BAMT’’). A general term to refer to in vitro
diagnostic tests that assess for the presence of tuberculosis (‘‘TB’’) infection with Myobacterium
tuberculosis. This term includes, but is not limited to, IFN- g release assays (‘‘IGRA’’).
B. The Facility shall conduct an annual tuberculosis risk assessment in accordance with the Centers
for Disease Control guidelines to guide the Facility’s infection control policies and procedures related
to the appropriateness and frequency of tuberculosis screening and other tuberculosis related measures
to be taken.
C. Baseline Status.
1. The Facility shall determine the baseline status of all staff according to current Centers for
Disease Control and Departmental Tuberculosis guidelines.
2. Tuberculosis Screening. All staff within three (3) months prior to Patient contact shall have a
baseline two-step Tuberculin Skin Test (‘‘TST’’) or a single Blood Assay for Mycobacterium
tuberculosis (‘‘BAMT’’). If a newly employed staff or volunteer has had a documented negative TST
or a BAMT result within the previous twelve (12) months, a single TST (or the single BAMT) can be
administered and read to serve as the baseline prior to Patient contact.
D. Post Exposure. After known exposure to a person with potentially infectious tuberculosis disease
without use of adequate personal protection, the tuberculosis status of all staff shall be determined in a
manner prescribed in the Centers for Disease Control and Department’s most current tuberculosis
guidelines.
E. Annual Tuberculosis Training. All staff shall receive annual training regarding tuberculosis to
include risk factors and signs and symptoms of tuberculosis disease. The annual tuberculosis training
shall be documented in a staff record and maintained at the Facility.
F. Serial Screening. The Facility shall follow the Centers for Disease Control and Department’s
most current tuberculosis guidelines related to serial screening.
1703. Tuberculosis Screening for Patients (I).
A. At baseline, Patients in Residential Facilities shall have evidence of a two-step tuberculin skin test
or single Blood Assay for Mycobacterium tuberculosis. If the Patient in a Residential Facility has a
documented negative tuberculin skin test (at least single-step) within the previous twelve (12) months,
the Patient shall have only one (1) tuberculin skin test or single Blood Assay for Mycobacterium
tuberculosis to establish a baseline status.
B. Patients in Residential Facilities shall have at least the first step within thirty (30) days prior to
admission and no later than forty-eight (48) hours after admission.
C. Patients in the Opioid Treatment Program shall receive the first step of the two-step tuberculin
test within seventy-two (72) hours of admission to the Facility. The second step of the two-step
tuberculin skin test must be administered within the next seven to fourteen (7 to 14) days.
D. Patients with Positive Tuberculosis Results.
1. Patients with a baseline positive or newly positive test result for Mycobacterium tuberculosis
infection (i.e., tuberculosis skin test or Blood Assay for Mycobacterium Tuberculosis) or documenta-
tion of treatment for latent tuberculosis infection, tuberculosis disease or signs or symptoms of
tuberculosis, e.g., cough, weight loss, night sweats, fever, shall have a chest radiograph performed
immediately to exclude tuberculosis disease (or evaluate an interpretable copy taken within the
previous three (3) months). Routine repeat chest radiographs are not required unless symptoms or
signs of TB tuberculosis disease develop or unless recommended by a Physician. These Patients will
be evaluated for the need for treatment of TB tuberculosis disease or latent tuberculosis infection
and will be encouraged to follow the recommendations made by a Physician with tuberculosis
expertise (i.e., the Department’s Tuberculosis Control program).
2. Patients who are known or suspected to have tuberculosis disease shall be transferred from the
Facility if the Facility does not have an Airborne Infection Isolation room, required to undergo
evaluation by a Physician, and permitted to return to the Facility only with approval by the
Department’s Tuberculosis Control program.
1704. Housekeeping (II).
A. The Facility and its grounds shall be neat, clean, free of vermin, and free of offensive odors.
B. Interior housekeeping shall at a minimum include:
1. Cleaning each specific area of the Facility;
2. Cleaning and disinfection, as needed, of equipment used and/or maintained in each area,
appropriate to the area and the equipment’s purpose or use;
3. Chemicals indicated as harmful on the product label, cleaning materials and supplies shall be
in locked storage areas and inaccessible to Patients; and
4. During use of chemicals indicated as harmful on the product label, cleaning materials and
supplies shall be in direct possession of the Staff member and monitored at all times.
C. Exterior housekeeping shall at a minimum include:
1. Cleaning of all exterior areas, such as porches and ramps, and removal of safety impediments
such as water, snow, and ice; and
2. Keeping Facility grounds free of weeds, rubbish, overgrown landscaping, and other potential
breeding sources for vermin.
1705. Infectious Waste (I).
Accumulated waste, including all contaminated sharps, dressings, pathological, and/or similar infec-
tious waste, shall be disposed of in a manner compliant with R.61–105, Infectious Waste Management,
and the OSHA Bloodborne Pathogens Standard.
1706. Pets (II).
A. Healthy animals that are free of fleas, ticks, and intestinal parasites, and have been examined by
a veterinarian prior to entering the Facility, have received required inoculations, if applicable, and that
present no apparent threat to the health, safety, and well-being of the Patients, shall be permitted in
the Facility, provided they are sufficiently fed, and cared for, and that the pets and their housing and
food containers are kept clean.
B. Pets shall not be allowed near Patients who have allergic sensitivities to pets, or for other
reasons, such as Patients who do not wish to have pets near them.
C. Pets shall not be allowed in the kitchen area. Pets shall be permitted in Patient dining and
activities areas only during times when food is not being served. If the dining and activities area is
adjacent to a food preparation or storage area, those areas shall be effectively separated by walls and
closed doors while pets are present.
1707. Clean and Soiled Linen and Clothing for Residential Facilities (II).
A. Clean Linen and Clothing.
1. A supply of clean, sanitary linen and clothing shall be available at all times;
2. In order to prevent the contamination of clean linen and clothing by dust or other airborne
particles or organisms, clean linen and clothing shall be stored and transported in a sanitary manner,
for example, enclosed and covered; and
3. Clean linen and clothing shall be separated from storage for other purposes.
B. Soiled Linen and Clothing.
1. Soiled linen and clothing shall not be sorted, rinsed, or washed outside of the laundry service
area;
2. Provisions shall be made for collecting, transporting, and storing soiled linen and clothing;
3. Soiled linen and clothing shall be kept in enclosed, covered, and leak proof containers; and
4. Laundry operations shall not be conducted in Patient rooms, dining rooms, or in locations
where food is prepared, served, or stored. Patients may sort, rinse, and handwash their own soiled,
delicate, personal items, e.g., pantyhose, underwear, socks, handkerchiefs, clothing, accessories,
heirloom linens, needlepoint, crocheted, or knitted pillows or pillowcases, or other similar items
personally owned and cared for by, in a private bathroom or sink, provided the practice does not
create a safety hazard, e.g. water on the floor.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 1700 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 1800. QUALITY IMPROVEMENT PROGRAM (II)
A. Facilities shall maintain a written, implemented Quality Improvement Program that provides
effective self-assessment and implementation of changes designed to improve the treatment/care/ser-
vices provided by the Facility.
B. The Quality Improvement Program, at a minimum, shall:
1. Establish desired outcomes and the criteria by which policy and procedure effectiveness is
regularly, systematically, and objectively accomplished;
2. Identify, evaluate, and determine the causes of any deviation from the desired outcomes;
3. Identify the action taken to correct deviations and prevent future deviation, and the person(s)
responsible for implementation of these actions;
4. Establish ways to measure the quality of Patient care and Staff performance, as well as the
degree to which the policies and procedures are followed;
5. Analyze the appropriateness of Individual Plans of Care and the necessity of treat-
ment/care/services rendered;
6. Analyze the effectiveness of the fire plan;
7. Analyze all incidents and accidents to include Patient deaths;
8. Analyze any infection, epidemic outbreaks, or other unusual occurrences which threaten the
health, safety, or well-being of the Patients; and
9. Establish a systematic method of obtaining feedback from Patients and other interested
persons, e.g., family members and peer organizations, as expressed by the level of satisfaction with
treatment/care/services received.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 1800 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 1900. DESIGN AND CONSTRUCTION
1901. Codes and Standards.
All Facilities shall be planned, designed, and equipped to provide and promote the health, safety, and
well-being of each Patient. Facility design shall be such that all Patients have access to required services.
1902. Local and State Codes and Standards (II).
A. Facilities shall comply with provisions of the codes officially adopted by the South Carolina
Building Codes Council and the South Carolina State Fire Marshal applicable to the type of Facility.
No Facility shall be licensed unless the Department has assurance that responsible local zoning and
building officials have approved the Facility for code compliance.
B. All Facilities shall meet the construction codes and regulations for the building and its essential
equipment and systems in effect at the time the License was issued unless specifically required
otherwise in writing by the Department.
C. Facilities shall ensure all additions, alterations, or renovations meet the codes, regulations, and
requirements in effect at the time of the plan’s approval.
D. Any Facility that closes or has its License revoked and for which application for licensure is
made at the same site shall be considered a new building and shall meet the current codes, regulations,
and requirements for the building and its essential equipment and systems in effect at the time of
application for licensing.
1903. Submission of Plans and Specifications (II).
A. Prior to construction for new buildings, additions, major alterations or replacement to existing
buildings, when a building is licensed for the first time, when a building changes License type, or a
Facility increases occupant load/licensed capacity, plans and specifications shall be submitted to the
Department for review, unless otherwise agreed to with the Department. Final plans and specifications
shall be prepared by an architect and/or engineer registered in South Carolina and shall bear their
seals and signatures. Architectural plans shall also bear the seal of a South Carolina registered
architectural corporation. These submissions shall be made in at least three (3) stages: schematic,
design development, and final. All plans shall be drawn to scale with the title, stage of submission, and
date shown thereon. Any construction changes from the approved documents shall be approved by the
Department. Construction work shall not commence until a construction plan approval has been
received from the Department. During construction the owner and/or Licensee shall employ a
registered architect and/or engineer for supervision and Inspections.
B. The Facility shall submit plans and specifications to the Department for review and approval for
projects that have an effect on:
1. The function of a space;
2. The accessibility to or of an area;
3. The structural integrity of the Facility;
4. The active and/or passive fire safety systems;
5. Doors;
6. Walls;
7. Ceiling system assemblies;
8. Exit corridors;
9. Life safety systems; or
10. That increase the occupant load or capacity of the Facility.
C. Cosmetic changes utilizing paint, wall covering, floor covering, etc., that are required to have a
flame-spread rating or other safety criteria shall be documented with copies of the documentation and
certifications, kept on file at the Facility, and made available to the Department.
D. All subsequent addenda, change orders, field orders, and documents altering the Department
review must be submitted. Any substantial deviation from the accepted documents shall require written
notification, review, and re-approval from the Department.
1904. Construction Inspections.
Construction work that violates applicable codes or standards shall be brought into compliance. All
projects shall obtain all required permits from the locality having jurisdiction. Construction without a
proper permit shall not be inspected by the Department.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 1900 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 2000. FIRE PROTECTION, PREVENTION, AND LIFE SAFETY (I)
A. Facilities with six (6) or more licensed Residential beds shall have a partial, manual, automatic,
supervised fire alarm system. The Facility shall arrange the system to transmit an alarm automatically
to a third party. The alarm system shall notify by audible and visual alarm all areas and floors of the
building. The alarm system shall shut down central recirculation systems and outside air units that
serve the area(s) of alarm origination as a minimum.
B. For Residential Facilities only, all fire, smoke, heat, sprinkler flow, and manual fire alarming
devices shall be connected to and activate the main fire alarm system when activated.
C. The fire-resistive ratings for the various structural components shall comply with the applicable
code(s) in Section 1900. Fire-resistive ratings of various materials and assemblies not specifically listed
in the codes can be found in publications of recognized testing agencies such as Underwriters
Laboratories - Building Materials List and Underwriters Laboratories - Fire Resistance Directory.
D. The Facility shall not have single and multi-station smoke alarms.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 2000 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 2100. [RESERVED]
HISTORY: Reserved by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 2100 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 2200. [RESERVED]
HISTORY: Reserved by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 2200 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 2300. [RESERVED]
HISTORY: Reserved by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 2300 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 2400. ELECTRICAL
2401. Receptacles (II).
A. Patient Room. Each Patient room shall have duplex grounding type receptacles located to
include one (1) at the head of each bed.
B. Corridors. Duplex receptacles for general use shall be installed approximately fifty (50) feet
apart in all corridors and within twenty-five (25) feet of the ends of corridors.
2402. Ground Fault Protection (I).
A. Ground fault circuit-interrupter protection shall be provided for all outside receptacles and
bathrooms.
B. The Facility shall provide ground fault circuit-interrupter protection for any receptacles within
six (6) feet of a sink or any other wet location. If the sink is an integral part of the metal splashboard
grounded by the sink, the entire metal area is considered part of the wet location.
2403. Exit Signs (I).
A. In Facilities licensed for six (6) or more beds, required exits and ways to access thereto shall be
identified by electrically-illuminated exit signs.
B. Changes in egress direction shall be marked with exit signs with directional arrows.
C. Exit signs in corridors shall be provided to indicate two (2) directions of exit.
2404. Emergency Electric Service (I).
Emergency electric services shall be provided as follows:
A. Exit lights, if required;
B. Exit access corridor lighting;
C. Illumination of means of egress; and
D. Fire detection and alarm system, if required.
2405. Emergency Generator Service.
A. Residential Facilities shall have an emergency generator and shall provide certification that
construction and installation of emergency generator service complies with requirements of all adopted
state, federal, or local codes, ordinances, and regulations.
B. Residential Facilities shall have an emergency generator that provides emergency electrical
service during interruption of the normal electrical service and shall be provided to the distribution
system as follows:
1. Exit lights and exit directional signs;
2. Exit access corridor lighting;
3. Lighting of means of egress and Staff work areas;
4. Fire detection and alarm systems;
5. In Patient care areas;
6. Signal system;
7. Equipment necessary for maintaining telephone service;
8. Elevator service that will reach every Patient floor when rooms are located on other than the
ground floor;
9. Fire pump (if applicable);
10. Equipment for heating and cooling Patient rooms;
11. Public restrooms;
12. Essential mechanical equipment rooms;
13. Battery-operated lighting and a receptacle in the vicinity of the emergency generator;
14. Alarm systems, water flow alarm devices, and alarms required for medical gas systems; and
15. Patient records when solely electronically based.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 2400 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 2500. [RESERVED]
HISTORY: Reserved by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 2500 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 2600. PHYSICAL PLANT
2601. Facility Accommodations and Floor Area (II).
A. Residential Facilities shall provide sufficient living arrangements for all Patients, including quiet
reading, study, relaxation, entertainment, or recreation.
B. Residential Facilities shall meet minimum square footage requirements as follows: (II)
1. Twenty (20) square feet per licensed bed of living and recreational areas combined, excluding
bedrooms, halls, kitchens, dining rooms, bathrooms, and rooms not available to the Patients. In
Facilities for parents with children, there shall be at least twenty (20) square feet per licensed bed
and ten (10) square feet per child of living and recreational areas together.
2. Fifteen (15) square feet of floor space in the dining area per licensed bed. In Facilities for
parents with children, dining space shall accommodate fifteen (15) square feet per licensed bed and
seven and a half (7.5) square feet per child.
C. Residential Facilities shall not require Patients to ambulate from one site to another outside the
building and shall not impede Patients from ambulating from one site to another due to the presence
of physical barriers.
D. Residential Facilities shall make accommodations available to meet group needs of Patients and
their visitors.
E. Residential Facilities shall ensure visual and auditory privacy between Patients and Staff and
Volunteers.
2602. Design (I).
Facilities shall be planned, designed, and equipped to provide and promote the health, safety, and
well-being of each Patient. Facility design shall be such that all Patients have access to required services.
There shall be two hundred (200) gross square feet per licensed bed in Residential Facilities ten (10)
beds or less, and an additional one hundred (100) gross square feet per licensed bed for each licensed
bed over ten (10).
2603. Furnishings and Equipment (I).
A. Facilities shall ensure the physical plant is free of fire hazards and impediments to fire
prevention.
B. Facilities shall not have any portable electric or unvented fuel heaters.
C. Facilities shall ensure that fireplaces and fossil-fuel stoves have partitions, screens, or other
means to prevent burns. Facilities shall ensure that fireplaces are vented to the outside and shall
prohibit ‘‘unvented’’ type gas logs. Facilities shall ensure that gas fireplaces have a remote gas shutoff
within the room but not inside the fireplace.
2604. Exits (I).
A. If exit doors and cross-corridor doors are locked, the requirements under Special Locking
Arrangements shall be met as applicable to the code listed in Section 1900.
B. Facilities shall maintain halls, corridors, and all other means of egress from the building free of
obstructions.
C. Facilities shall not assign Patients needing physical or verbal assistance to exit the building to
rooms located above or below the floor of exit discharge.
D. Facilities shall ensure that each Patient room opens directly to an approved exit access corridor
without passage through another occupied space or has an approved exit directly to the outside at
grade level and accessible to a public space free of encumbrances. When two (2) Patient rooms share a
common ‘‘sitting’’ area, the ‘‘sitting’’ area shall open onto the exit access corridor.
2605. Water Supply and Hygiene (II).
Facilities shall ensure that Patient and Staff handwashing lavatories, and Patient showers and tubs
are supplied with hot and cold water at all times.
2606. Temperature Control (I).
A. Facilities shall ensure that plumbing fixtures accessible to Patients and requiring hot water to
have a water supply that is thermostatically controlled to a temperature of at least one hundred (100)
degrees Fahrenheit and not to exceed one hundred and twenty (120) degrees Fahrenheit at the
fixture.
B. Residential Facilities shall ensure that water heaters provide at least six (6) gallons of water per
hour per bed at the above temperature range. (II)
C. Hot water supplied to the kitchen equipment/utensil washing sink shall be supplied at one
hundred and twenty (120) degrees Fahrenheit provided all kitchen equipment/utensils are chemically
sanitized. For those Facilities sanitizing with hot water, the sanitizing compartment of the kitchen
equipment and utensil washing sink shall be capable of maintaining the water at a temperature of at
least one hundred and seventy one (171) degrees Fahrenheit.
D. Hot water provided for washing linen and clothing shall not be less than one hundred and sixty
(160) degrees Fahrenheit. Should chlorine additives or other chemicals which contribute to the margin
of safety in disinfecting linen/clothing be a part of the washing cycle, the minimum hot water
temperature shall not be less than one hundred and ten (110) degrees Fahrenheit, provided hot air
drying is used. (II)
2607. Cross-connections (I).
Facilities shall ensure that there are no cross-connections in plumbing between safe and potentially
unsafe water supplies. Facilities shall ensure water is delivered at least two (2) delivery pipe diameters
above the rim or points of overflow to each fixture, equipment, and service unless protected against
back-siphonage by approved vacuum breakers or other approved back-flow preventers. Facilities shall
ensure that all faucets and fixtures which may be attached to a hose have an approved vacuum breaker
or other approved back-flow preventer.
2608. Wastewater Systems (I).
A. Residential Facilities shall ensure the wastewater system for commercial kitchens is in accordance
with R.61–25, Retail Food Establishments.
B. Facilities shall dispose of liquid waste in a wastewater system approved by the local authority.
2609. Electric Wiring (I).
Facilities shall ensure that a licensed electrician, registered engineer, or certified building inspector
inspects the electric wiring at least annually.
2610. Panelboards (II).
Facilities shall label the panelboard directory to conform to the actual room numbers or designations
and shall maintain clear access to the panelboard.
2611. Lighting.
A. Facilities shall maintain lighting in spaces occupied by persons, machinery, and equipment
within buildings, approaches to buildings, and parking lots. (II)
B. Facilities shall provide artificial light with sufficient illumination for reading, observation, and
activities.
C. Residential Facilities shall maintain general lighting in all parts of Patients’ rooms, and shall
provide at least one (1) light fixture for night lighting in each Patient room. Residential Facilities shall
provide a reading light to each Patient.
D. Facilities shall maintain lighted hallways, stairs, and all other means of egress at all times.
2612. Heating, Ventilation, and Air Conditioning (II).
A. Facilities shall ensure that a certified or licensed technician inspects the heating, ventilation, and
air conditioning system at least annually.
B. Facilities shall maintain a temperature between seventy-two (72) and seventy-eight (78) degrees
Fahrenheit in Patient areas.
C. Facilities shall ensure that heating, ventilation, and air conditioning supplies and return grills
are installed at least three (3) feet away from a smoke detector. (I)
D. Facilities shall ensure that heating, ventilation, and air conditioning grills are not installed in the
floors.
E. Facilities shall ensure that intake air ducts are filtered and maintained to prevent the entrance of
dust, dirt, and other contaminating materials. Facilities shall ensure discharge from the heating,
ventilation, and air conditioning system does not irritate Patients, Staff, and Volunteers.
F. Facilities shall have operable windows or approved mechanical ventilation in every bathroom
and restroom.
G. Facilities shall ensure all kitchen areas are ventilated to prevent excessive heat, steam, condensa-
tion, vapors, smoke, and fumes.
2613. Patient Rooms.
A. Residential Facilities shall provide the following equipment in each Patient room for each
Patient:
1. A comfortable single bed having a mattress with moisture-proof cover, sheets, blankets, pillow
and pillowcases. Roll-away type beds, cots, bunkbeds, and folding beds are not permitted. Facilities
are permitted to remove a Patient bed and place the mattress on a platform or pallet, or utilize a
recliner, upon approval by the Physician or other Authorized Healthcare Provider and documenta-
tion is provided in the Individual Plan of Care. (II)
2. A closet or wardrobe, a bureau consisting of at least three (3) drawers, and a compartmental-
ized bedside table or nightstand to adequately accommodate each Patient’s personal clothing,
belongings, and toilet articles. Facilities are permitted to utilize built-in storage.
3. A comfortable chair for each Patient occupying the room. If the available square footage of the
Patient room will not accommodate a chair for each Patient or if the provision of multiple chairs
impedes Patient ability to freely and safely move about within their room, Facilities shall provide at
least one (1) chair and make additional chairs available for temporary use in the Patient’s room for
visitors.
B. Facilities that use hospital-type beds shall maintain at least two (2) lockable casters on each bed,
located either diagonally or on the same side of the bed.
C. Facilities shall not place beds in corridors, solaria, or other locations not designated as Patient
room areas. (I)
D. Facilities shall ensure Patient rooms have a maximum of three (3) beds. Facilities with mothers
with children shall ensure Patient rooms have a maximum of one (1) licensed bed and two (2) cribs or
beds. (II)
E. Facilities shall not have any Patient rooms in a basement.
F. Facilities shall not provide access to a Patient room through another Patient room, toilet,
bathroom or kitchen.
G. Facilities shall provide bed pans, urinals, hot water bottles, and any other equipment necessary
to meet Patient needs. Facilities are permitted to have portable toilets in Patient rooms only at night or
in case of temporary illness, and shall keep them stored at all other times. Facilities are permitted to
permanently position a portable toilet at a Patient’s bedside if the toilet is sanitary and the Patient room
is private and of a sufficient size. (II)
H. Facilities are permitted to utilize side rails when required for safety and when ordered by a
Physician or other Authorized Healthcare Provider. (II)
I. Facilities shall ensure privacy when personal care is being given to a Patient in a semi-private
room.
J. Facilities shall consider Patient compatibility in the assignment of rooms for which there is
multiple occupancy.
K. Facilities shall have at least one (1) private room available in the Facility in order to provide
assistance in addressing Patient compatibility issues, Patient preferences, and accommodations for
Patients with communicable disease.
2614. Patient Room Floor Area.
A. Except for Residential Facilities of five (5) beds or less, each Patient room is considered a tenant
space and shall be enclosed by one (1)-hour fire-resistive construction with a twenty (20)-minute fire-
rated door, opening onto an exit access corridor. (I)
B. Each Patient room shall be an outside room with an outside window or door for exit in case of
emergency. This window or door may not open onto a common screened porch. (I)
C. The Patient room floor area is a usable or net area and does not include wardrobes (built-in or
freestanding), closets, or the entry alcove to the room. The following allowance of floor space shall be
as a minimum: (II)
1. Rooms for only one (1) Patient: one hundred (100) square feet;
2. Rooms for more than one (1) Patient: eighty (80) square feet per Patient.
3. In Facilities for mothers with children, rooms for Patient and child: eighty (80) square feet per
licensed bed and forty (40) square feet per child with a maximum of two (2) children per Patient.
When a bed is required in lieu of a crib for a child, the square footage shall be fifty (50) square feet
per child.
D. Facilities shall maintain at least three (3) feet between beds. (II)
2615. Bathrooms and Restrooms (II).
A. Privacy shall be provided at toilets, urinals, bathtubs, and showers.
B. An adequate supply of toilet tissue shall be maintained in each bathroom.
C. There shall be at least one (1) handwash lavatory adjacent to each toilet. Liquid soap shall be
provided in public restrooms and bathrooms used by more than one (1) Patient. Communal use of bar
soap is prohibited. A sanitary individualized method of drying hands shall be available at each lavatory.
D. Easily cleanable receptacles shall be provided for waste materials. Such receptacles in toilet
rooms for women shall be covered. The Facility shall ensure receptacles are non-combustible or fire
resistant as required by building codes reference in Section 1900.
E. All bathroom floors shall be entirely covered with an approved nonabsorbent covering. Walls
shall be nonabsorbent, washable surfaces to the highest level of splash.
F. There shall be a mirror above each bathroom lavatory for Patients’ grooming.
G. In Residential Facilities:
1. Facilities shall provide an ample number of toilets to serve the needs of the Patients Staff
members, Volunteers, and the public. Facilities shall provide Patients with a minimum of one (1)
toilet for each six (6) licensed beds or fraction thereof.
2. All bathtubs, toilets, and showers used by Patients shall have approved grab bars securely
fastened in a usable fashion.
3. There shall be one (1) bathtub or shower for each eight (8) beds or fraction thereof.
4. Separate bathrooms shall be provided for Staff members, Volunteers, and the public.
5. Toilet facilities shall be at or adjacent to the kitchen for kitchen employees.
6. Soap, bath towels, and washcloths shall be provided to each Patient as needed. Bath linens
assigned to specific Patients may not be stored in centrally-located bathrooms. Provisions shall be
made for each Patient to properly keep their bath linens in their room, such as, on a towel hook or
bar designated for each Patient occupying that room, or bath linens to meet Patient needs shall be
distributed as needed, and collected after use and stored properly, per Section 1707.
H. Facilities shall have bathrooms and restrooms equipped for handicapped persons as required by
building codes referenced in Section 1900.
2617. Patient Care Unit and Station for Medical Withdrawal Management Programs (II).
A. Each Patient care unit shall have a Patient care station.
B. A Patient care unit shall contain not more than forty-four (44) licensed beds; and the Patient
care station shall not be more than one hundred fifty (150) feet from a Patient room, and shall be
located and arranged to permit visual observation of the unit corridor(s).
C. Each Patient care station shall contain separate spaces for the storage of wheelchairs and general
supplies/equipment for that station.
D. There shall be at, or near each Patient care station, a separate medicine preparation room with
a cabinet with one or more locked sections for Controlled Substances, work space for preparation of
medicine, and a sink. As an alternative, a medicine preparation area with counter, cabinet space, and a
sink shall be required on those units where there is:
1. A unit dose system in which final Medication preparation is not performed on the Patient care
station; or
2. A twenty-four (24) hour pharmacy on the premises; or
3. Procedures that preclude Medication preparation at the Patient care station.
2618. Doors (II).
A. All Patient rooms and bathrooms and restrooms shall have opaque doors for the purpose of
privacy.
B. All glass doors, including sliding or patio type doors shall have a contrasting or other indicator
that causes the glass to be observable.
C. Bathroom and restroom door widths shall be not less than thirty-six (36) inches.
D. Doors to Patient occupied rooms shall be at least thirty-six (36) inches wide.
E. Doors that have locks shall be unlockable and openable with one action.
F. If Patient room doors are lockable, there shall be provisions for emergency entry. There shall
not be locks that cannot be unlocked and operated from inside the room.
G. All Patient room doors shall be solid-core.
2619. Elevators (II).
Facilities shall ensure that a certified elevator inspector inspects and tests elevators upon installation
prior to first use and annually thereafter.
2620. Screens (II).
Facilities shall equip windows, doors, and openings intended for ventilation with insect screens.
2621. Janitor’s Closet (II).
Residential Facilities shall maintain a lockable janitor’s closet equipped with a mop sink or receptor
and space for the storage of supplies and equipment.
2622. Storage Areas.
A. Facilities shall provide adequate general storage areas for Patient and Staff and Volunteer
belongings, equipment, and supplies.
B. Facilities shall ensure that areas used for storage of combustible materials and storage areas
exceeding one hundred (100) square feet in area are equipped with a National Fire Protection
Association-approved automatic sprinkler system. (I)
C. In storage areas provided with a sprinkler system, a minimum vertical distance of eighteen (18)
inches shall be maintained between the top of stored items and the sprinkler heads. The tops of
storage cabinets and shelves attached to or built into the perimeter walls may be closer than eighteen
(18) inches below the sprinkler heads. In non-sprinklered storage areas, there shall be at least twenty-
four (24) inches of space from the ceiling. (I)
D. All ceilings, floor assemblies, and walls enclosing storage areas of one hundred (100) square feet
or greater shall be of not less than one (1) hour fire-resistive construction with three-fourths (3/4) hour
fire-rated door(s) and closer(s). (I)
E. Facilities shall ensure that storage buildings on the premises meet the applicable code listed in
Section 1900 regarding distance from the licensed building. An appropriate controlled environment
shall be provided if necessary for storage of items requiring such an environment.
F. Facilities shall ensure that items stored in mechanical rooms are located away from mechanical
equipment and are not a type of storage that might create a fire or other hazard. (I)
G. Facilities shall not store supplies and equipment directly on the floor. Facilities shall not store
supplies and equipment susceptible to water damage and contamination under sinks or other areas
with a propensity for water leakage.
H. Facilities licensed for more than fifteen (15) beds shall maintain a soiled linen storage room
designed, enclosed, and used solely for that purpose and equipped with mechanical exhaust directly to
the outside.
2623. Telephone Service.
A. Facilities shall provide at least one (1) telephone on each floor of the Facility with at least one (1)
active main or fixed-line telephone service available.
B. Facilities shall provide at least one (1) telephone on each floor for Staff members and Volunteers
to conduct routine business of the Facility and to summon assistance in the event of an emergency. The
Facility shall ensure Patients have privacy when using the telephone.
2624. Location.
A. Facilities shall ensure that roads serving the Facility are passable at all times.
B. Facilities shall provide parking space to meet the needs of Patients, Staff, Volunteers, and
visitors.
C. Facilities shall maintain adequate access to and around the building for firefighting equipment.
(I)
D. Facilities providing an Opioid Treatment Program shall not operate within five hundred (500)
feet of:
1. The property line of a church;
2. The property line of a public or private elementary or secondary school;
3. A boundary of any Residential district;
4. A public park adjacent to any Residential district; or
5. The property line of a lot devoted to Residential use.
2625. Outdoor Area.
A. Facilities shall ensure outdoor areas where unsafe, unprotected physical hazards exist are
enclosed by a fence or a natural barrier of a size, shape, and density that effectively impedes travel to
the hazardous area. (I)
B. Facilities shall protect mechanical and equipment rooms that open to the outside of the Facility
from unauthorized individuals.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 2600 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 2700. SEVERABILITY
In the event that any portion of this regulation is construed by a court of competent jurisdiction to be
invalid, or otherwise unenforceable, such determination shall in no manner affect the remaining
portions of this regulation, and they shall remain in effect, as if such invalid portions were not
originally a part of this regulation.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 2700 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025.
SECTION 2800. GENERAL
Conditions that have not been addressed in this regulation shall be managed in accordance with the
best practices as interpreted by the Department.
HISTORY: Amended by SCSR 44–6 Doc. No. 4954, eff June 26, 2020. Transferred from 61–93 § 2800 by SCSR
49–5 Doc. No. 5352, eff May 23, 2025