Code of Federal Regulations, Title 21, Food and Drugs, PT. 1-99, Revised as of April 1, 2009

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Office of the Federal Register (U S )
Government Printing Office, 2009 - Law - 519 pages
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Contents

CHAPTER IFOOD AND DRUG
7
Title
21
statements Requirements To Submit Prior Notice
27
ADMINISTRATION DEPARTMENT OF HEALTH AND HUMAN SERVICES
55
Part Page 1 General enforcement regulations 5
61
Product jurisdiction
67
Organization
72
Enforcement policy
78
Protection of privacy
230
Environmental impact considerations
247
United States and The European Community
258
Protection of human subjects
291
Financial disclosure by clinical investigators
303
Institutional Review Boards
306
Good laboratory practice for nonclinical labora
316
tory studies
322

Administrative practices and procedures
87
Electronic records electronic signatures
122
Formal evidentiary public hearing
125
Public hearing before a public board of inquiry
143
Public hearing before a public advisory committee
148
Public hearing before the Commissioner
175
Regulatory hearing before the Food and Drug Ad ministration
177
Civil money penalties hearings
183
Standards of conduct and conflicts of interest
197
Public information
199
Patent term restoration
329
Part Page
337
Color additive petitions
344
Listing of color additives exempt from certifi
351
Listing of color additives subject to certification
401
Color additive certification
441
General specifications and general restrictions
447
Listing of certified provisionally listed colors
454
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Published by the Office of the Federal Register, National Archives and Records Administration. Official U.S. Government Edition.

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