modify provisions related to the practice of pharmacy.
What changed between versions
Added and updated definitions for 'Biological product' and 'Interchangeable biological product' to reference specific federal standards and dates (January 1, 2018 for biological products; January 1, 2025 for nonprescription drug regulations).
Added new definitions for 'Drug device' and 'Equivalent drug product' to clarify what equipment and products count as part of medication management systems.
Updated the definition of 'Nonprescription drugs' to include specific federal law references (21 U.S.C. § 352 and § 353) with January 1, 2025 effective dates, clarifying what drugs can be sold without prescriptions.
Added 'Patient counseling' and 'Pharmaceutical care' definitions to clarify the pharmacist's role in ensuring proper drug use and achieving therapeutic outcomes.
Added 'Registered pharmacy technician' definition to clarify the scope of tasks pharmacy technicians can perform under pharmacist supervision.