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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 A - General |
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Part 25 - Environmental Impact Considerations |
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Subpart C - Categorical Exclusions |
| § 25.30 - General. |
| § 25.31 - Human drugs and biologics. |
| § 25.32 - Foods, food additives, and color additives. |
| § 25.33 - Animal drugs. |
| § 25.34 - Devices and electronic products. |
| § 25.35 - Tobacco product applications. |
| § 25.31a - Environmental assessment for proposed approvals of FDA-regulated products—Format 1. |
| § 25.31b - Environmental assessment for withdrawals of approval and other restrictions—Format 2. |
| § 25.31c - Environmental assessment format for extramural contracts, grants, or other research agreements—Format 3. |
| § 25.31d - Environmental assessment for establishment of tolerances or action levels—Format 4. |
| § 25.31e - Environmental assessment for destruction of condemned, enjoined, detained, or recalled articles—Format 5. |