21 CFR Part 25
PART 25—ENVIRONMENTAL IMPACT CONSIDERATIONS
- PART 25—ENVIRONMENTAL IMPACT CONSIDERATIONS
- Chapter I—Food and Drug Administration, Department of Health and Human Services › Subchapter A—General
- Subpart A—General Provisions
- § 25.1 Purpose.
- § 25.5 Terminology.
- § 25.10 Policies and NEPA planning.
- Subpart B—Agency Actions Requiring Environmental Consideration
- § 25.15 General procedures.
- § 25.16 Public health and safety emergencies.
- § 25.20 Actions requiring preparation of an environmental assessment.
- § 25.21 Extraordinary circumstances.
- § 25.22 Actions requiring the preparation of an environmental impact statement.
- 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.
- Subpart D—Preparation of Environmental Documents
- § 25.40 Environmental assessments.
- § 25.41 Findings of no significant impact.
- § 25.42 Environmental impact statements.
- § 25.43 Records of decision.
- § 25.44 Lead and cooperating agencies.
- § 25.45 Responsible agency official.
- Subpart E—Public Participation and Notification of Environmental Documents
- § 25.50 General information.
- § 25.51 Environmental assessments and findings of no significant impact.
- § 25.52 Environmental impact statements.
- Subpart F—Other Requirements
- § 25.60 Environmental effects abroad of major agency actions.
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