General

  1. Law
  2. CFR 21
  3. Food and Drugs
  4. Food and Drug Administration, Department of Health and Human Services
  5. General

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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
6

XXX

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
83-98

Parts 83-98 [Reserved]

Part
99

Dissemination of Information on Unapproved/New Uses for Marketed Drugs, Biologics, and Devices