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.