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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 E - Control of Components and Drug Product Containers and Closures |
| § 211.80 - General requirements. |
| § 211.82 - Receipt and storage of untested components, drug product containers, and closures. |
| § 211.84 - Testing and approval or rejection of components, drug product containers, and closures. |
| § 211.86 - Use of approved components, drug product containers, and closures. |
| § 211.87 - Retesting of approved components, drug product containers, and closures. |
| § 211.89 - Rejected components, drug product containers, and closures. |
| § 211.94 - Drug product containers and closures. |