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Section 34-23-32.1 - Adherence to FDA requirements under Federal Prescription Drug Marketing Act of 1987.

AL Code § 34-23-32.1 (2019) (N/A)
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Any requirements established by the FDA Guidelines, as required by the Federal Prescription Drug Marketing Act of 1987 (PDMA), as amended, specifically addressed in Sections 34-23-1 and 34-23-32, shall be adhered to by the affected parties.

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Section 34-23-32 - Manufacturer, bottler, packager, repackager, etc., of drugs.
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Section 34-23-32.2 - Revocation, suspension, etc., of license or certificate; non-disciplinary administrative penalty.