Current through Register Vol. 51, No. 24, December 2, 2024
Section 10.34.28.10 - Quality Assurance ProgramA. 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;(6) Preventative maintenance;(10) Drug procurement, delivery, and receipt;(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.Md. Code Regs. 10.34.28.10