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Title 21

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eCFR Content

Editorial codification of the general and permanent rules published in the Federal Register.

Title 21 Food and Drugs Part / Section
Chapter I Food and Drug Administration, Department of Health and Human Services 1 – 1299
Subchapter A General 1 – 99
Part 1 General Enforcement Regulations 1.1 – 1.980
Part 2 General Administrative Rulings and Decisions 2.5 – 2.125
Part 3 Product Jurisdiction 3.1 – 3.10
Part 4 Regulation of Combination Products 4.1 – 4.105
Part 5 Organization 5.1100 – 5.1110
Part 7 Enforcement Policy 7.1 – 7.87
Part 10 Administrative Practices and Procedures 10.1 – 10.206
Part 11 Electronic Records; Electronic Signatures 11.1 – 11.300
Part 12 Formal Evidentiary Public Hearing 12.1 – 12.159
Part 13 Public Hearing Before a Public Board of Inquiry 13.1 – 13.50
Part 14 Public Hearing Before a Public Advisory Committee 14.1 – 14.174
Part 15 Public Hearing Before the Commissioner 15.1 – 15.45
Part 16 Regulatory Hearing Before the Food and Drug Administration 16.1 – 16.120
Part 17 Civil Money Penalties Hearings 17.1 – 17.54
Part 19 Standards of Conduct and Conflicts of Interest 19.1 – 19.55
Part 20 Public Information 20.1 – 20.120
Part 21 Protection of Privacy 21.1 – 21.75
Part 25 Environmental Impact Considerations 25.1 – 25.60
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 26.0 – 26.81
Part 50 Protection of Human Subjects 50.1 – 50.56
Part 54 Financial Disclosure by Clinical Investigators 54.1 – 54.6
Part 56 Institutional Review Boards 56.101 – 56.124
Part 58 Good Laboratory Practice for Nonclinical Laboratory Studies 58.1 – 58.219
Part 60 Patent Term Restoration 60.1 – 60.46
Part 70 Color Additives 70.3 – 70.55
Part 71 Color Additive Petitions 71.1 – 71.37
Part 73 Listing of Color Additives Exempt from Certification 73.1 – 73.3129
Part 74 Listing of Color Additives Subject to Certification 74.101 – 74.3710
Part 80 Color Additive Certification 80.10 – 80.39
Part 81 General Specifications and General Restrictions for Provisional Color Additives for Use in Foods, Drugs, and Cosmetics 81.1 – 81.30
Part 82 Listing of Certified Provisionally Listed Colors and Specifications 82.3 – 82.2707a
Parts 83-98 [Reserved]
Part 99 Dissemination of Information on Unapproved/New Uses for Marketed Drugs, Biologics, and Devices 99.1 – 99.501