What Current Good Manufacturing Practice for Finished Pharmaceuticals requires
This regulation establishes the minimum requirements for methods, facilities, and controls used in the manufacturing, processing, packing, or holding of finished pharmaceuticals to…
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Pillar: Pharmaceuticals & Life Sciences · Authority: Food and Drug Administration, Department of Health and Human Services · Version: 1.0.0 · Last updated:
Primary source: https://www.ecfr.gov/current/title-21/chapter-I/subchapter-C/part-211
SHA-256 integrity: 91b3f4cdbabed04773af19b761b1c83216b17446b1e342ce5034d900ed4ffd45
Primary Citations — 7 traced to source
- 21 CFR § 211.1 - Scope
- 21 CFR § 211.22 - Responsibilities of quality control unit
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- Discovery (free): /api/v1/nodes/us-fda-21-cfr-211-cgmp-finished-pharmaceuticals.json — 6-field metadata
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