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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter C - Drugs: General |
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Part 211 - Current Good Manufacturing Practice for Finished Pharmaceuticals |
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Subpart F - Production and Process Controls |
| § 211.100 - Written procedures; deviations. |
| § 211.101 - Charge-in of components. |
| § 211.103 - Calculation of yield. |
| § 211.105 - Equipment identification. |
| § 211.110 - Sampling and testing of in-process materials and drug products. |
| § 211.111 - Time limitations on production. |
| § 211.113 - Control of microbiological contamination. |
| § 211.115 - Reprocessing. |