Code of Maryland Regulations (Last Updated: April 6, 2021) |
Title 10. Maryland Department of Health |
Part 4. |
Subtitle 34. BOARD OF PHARMACY |
Chapter 10.34.28. Automated Medication Systems |
Sec. 10.34.28.10. Quality Assurance Program
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A. The responsible pharmacist, in consultation with the health care facility, a related institution as defined in Health-General Article, §19-301, Annotated Code of Maryland, or a medical facility owned and operated by a group model health maintenance organization as defined in Health-General Article, §19.713.6, Annotated Code of Maryland, shall develop, maintain, and review annually a quality assurance program regarding the automated medication system that addresses, at minimum:
(1) A testing program which includes daily accuracy sampling that verifies the integrity of the system;
(2) Investigation of medication errors related to the automated medication system, and remedial actions taken;
(3) Review of discrepancies and transaction reports to identify patterns of inappropriate use and access;
(4) Review of the overall functioning of the system2;
(5) Security and access:
(6) Preventative maintenance;
(7) Sanitation;
(8) Storage conditions;
(9) Inventory of drugs;
(10) Drug procurement, delivery, and receipt;
(11) Record keeping;
(12) Proper labeling procedures; and
(13) Protocols in the event of a power outage or other situation in which the services of the system are interrupted, that include:
(a) A plan for insuring continuity of pharmacy services to patients; and
(b) A plan for system recovery.
B. The responsible pharmacist, in consultation with the health care facility, a related institution as defined in Health-General Article, §19-301, Annotated Code of Maryland, or a medical facility owned and operated by a group model health maintenance organization as defined in Health-General Article, §19.713.6, Annotated Code of Maryland, shall develop, maintain, and review annually a quality assurance program regarding the remote or decentralized automated medication system that addresses, at a minimum, system override management to include:
(1) A list of medications that can be overridden which is limited to starter doses; and
(2) Review of system overrides to ensure appropriate utilization.