Title 21--Food and Drugs

(This index contains parts 1 to 99)

CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES

Part  
1 General enforcement regulations
2 General administrative rulings and decisions
3 Product jurisdiction
5 Delegations of authority and organization
7 Enforcement policy
10 Administrative practices and procedures
11 Electronic records; electronic signatures
12 Formal evidentiary public hearing
13 Public hearing before a public board of inquiry
14 Public hearing before a public advisory committee
15 Public hearing before the Commissioner
16 Regulatory hearing before the Food and Drug Administration
17 Civil money penalties hearings
19 Standards of conduct and conflicts of interest
20 Public information
21 Protection of privacy
25 Environmental impact considerations
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
50 Protection of human subjects
54 Financial disclosure by clinical investigators
56 Institutional Review Boards
58 Good laboratory practice for nonclinical laboratory studies
60 Patent term restoration
70 Color additives
71 Color additive petitions
73 Listing of color additives exempt from certification
74 Listing of color additives subject to certification
80 Color additive certification
81 General specifications and general restrictions for provisional color additives for use in foods, drugs, and cosmetics
82 Listing of certified provisionally listed colors and specifications
83-98 [Reserved]
99 Dissemination of information on unapproved/new uses for marketed drugs, biologics, and devices

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