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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 F - Biologics |
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Part 600 - Biological Products: General |
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Subpart D - Reporting of Adverse Experiences |
| § 600.80 - Postmarketing reporting of adverse experiences. |
| § 600.81 - Distribution reports. |
| § 600.82 - Notification of a permanent discontinuance or an interruption in manufacturing. |
| § 600.90 - Waivers. |