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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 J - Records and Reports |
| § 211.180 - General requirements. |
| § 211.182 - Equipment cleaning and use log. |
| § 211.184 - Component, drug product container, closure, and labeling records. |
| § 211.186 - Master production and control records. |
| § 211.188 - Batch production and control records. |
| § 211.192 - Production record review. |
| § 211.194 - Laboratory records. |
| § 211.196 - Distribution records. |
| § 211.198 - Complaint files. |