Subchapter VII. General Authority

Part A. General Administrative Provisions

• 21 U.S.C. § 371 Regulations and Hearings
• 21 U.S.C. § 372 Examinations and Investigations
• 21 U.S.C. § 372a Transferred
• 21 U.S.C. § 373 Records
• 21 U.S.C. § 374 Inspection
• 21 U.S.C. § 374a Inspections Relating to Food Allergens
• 21 U.S.C. § 375 Publicity
• 21 U.S.C. § 376 Examination of Sea Food On Request of Packer; Marking Food With Results; Fees; Penalties
• 21 U.S.C. § 377 Revision of United States Pharmacopoeia; Development of Analysis and Mechanical and Physical Tests
• 21 U.S.C. § 378 Advertising of Foods
• 21 U.S.C. § 379 Confidential Information
• 21 U.S.C. § 379a Presumption of Existence of Jurisdiction
• 21 U.S.C. § 379b Consolidated Administrative and Laboratory Facility
• 21 U.S.C. § 379c Transferred
• 21 U.S.C. § 379d Automation of Food and Drug Administration
• 21 U.S.C. § 379d-1 Conflicts of Interest
• 21 U.S.C. § 379d-2 Policy On the Review and Clearance of Scientific Articles Published By Fda Employees
• 21 U.S.C. § 379d-3 Streamlined Hiring Authority
• 21 U.S.C. § 379d-3a Hiring Authority For Scientific, Technical, and Professional Personnel
• 21 U.S.C. § 379d-3b Strategic Workforce Plan and Report
• 21 U.S.C. § 379d-4 Reporting Requirements
• 21 U.S.C. § 379d-5 Guidance Document Regarding Product Promotion Using the Internet

Part B. Colors

• 21 U.S.C. § 379e Listing and Certification of Color Additives For Foods, Drugs, Devices, and Cosmetics

Part C. Fees

• Subpart 1. Freedom of Information Fees
• Subpart 2. Fees Relating to Drugs
• Subpart 3. Fees Relating to Devices
• Subpart 4. Fees Relating to Animal Drugs
• Subpart 5. Fees Relating to Generic New Animal Drugs
• Subpart 6. Fees Related to Food
• Subpart 7. Fees Relating to Generic Drugs
• Subpart 8. Fees Relating to Biosimilar Biological Products
• Subpart 9. Fees Relating to Outsourcing Facilities
• Subpart 10. Fees Relating to Over-The-Counter Drugs

Part D. Information and Education

• 21 U.S.C. § 379k Information System
• 21 U.S.C. § 379k-1 Electronic Format For Submissions
• 21 U.S.C. § 379l Education

Part E. Environmental Impact Review

• 21 U.S.C. § 379o Environmental Impact

Part F. National Uniformity For Nonprescription Drugs and Preemption For Labeling Or Packaging of Cosmetics

• 21 U.S.C. § 379r National Uniformity For Nonprescription Drugs
• 21 U.S.C. § 379s Preemption For Labeling Or Packaging of Cosmetics

Part G. Safety Reports

• 21 U.S.C. § 379v Safety Report Disclaimers

Part H. Serious Adverse Event Reports

• 21 U.S.C. § 379aa Serious Adverse Event Reporting For Nonprescription Drugs
• 21 U.S.C. § 379aa-1 Serious Adverse Event Reporting For Dietary Supplements

Part I. Reagan-Udall Foundation For the Food and Drug Administration

• 21 U.S.C. § 379dd Establishment and Functions of the Foundation
• 21 U.S.C. § 379dd-1 Location of Foundation
• 21 U.S.C. § 379dd-2 Activities of the Food and Drug Administration