Good manufacturing practices (GMP) guidelines for ... - Explore further
2021-11-9u2002·u2002Active Pharmaceutical Ingredients (API) and intermediates for pharmaceutical use (i.e. pharmaceutical, radiopharmaceutical, and biological) and those used to manufacture drugs for clinical trials are regulated under the Divisions 1A and 2, Part C of the Food and Drug Regulations.Division 1A, Part C of the Food and Drug Regulations defines activities for which Good Manufacturing Practices …
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