Code of Federal Regulations · Subchapter
Subchapter A — General
21 C.F.R. subch. A
- Part 1 General Enforcement Regulations
- Part 2 General Administrative Rulings And Decisions
- Part 3 Product Jurisdiction
- Part 4 Regulation Of Combination Products
- Part 5 Organization
- Part 7 Enforcement Policy
- Part 10 Administrative Practices And Procedures
- Part 11 Electronic Records; Electronic Signatures
- Part 12 Formal Evidentiary Public Hearing
- Part 13 Public Hearing Before A Public Board Of Inquiry
- Part 14 Public Hearing Before A Public Advisory Committee
- Part 15 Public Hearing Before The Commissioner
- Part 16 Regulatory Hearing Before The Food And Drug Administration
- Part 17 Civil Money Penalties Hearings
- Part 19 Standards Of Conduct And Conflicts Of Interest
- Part 20 Public Information
- Part 21 Protection Of Privacy
- Part 25 Environmental Impact Considerations
- Part 26 Mutual Recognition Of Pharmaceutical Good Manufacturing Practice Reports, Medical Device Quality System Audit Reports, And Certain Medical Device Product Evaluation Reports: United States And The European Community
- Part 50 Protection Of Human Subjects
- Part 54 Financial Disclosure By Clinical Investigators
- Part 56 Institutional Review Boards
- Part 58 Good Laboratory Practice For Nonclinical Laboratory Studies
- Part 60 Patent Term Restoration
- Part 70 Color Additives
- Part 71 Color Additive Petitions
- Part 73 Listing Of Color Additives Exempt From Certification
- Part 74 Listing Of Color Additives Subject To Certification
- Part 80 Color Additive Certification
- Part 81 General Specifications And General Restrictions For Provisional Color Additives For Use In Foods, Drugs, And Cosmetics
- Part 82 Listing Of Certified Provisionally Listed Colors And Specifications
- Part 99 Dissemination Of Information On Unapproved/new Uses For Marketed Drugs, Biologics, And Devices
- Part 83-98 Parts 83-98 [reserved]