Code of Federal Regulations Title 21 Food and Drugs: Parts 1 to 99: Revised As of April 1, 2011

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Government Printing Office, Jun 28, 2011 - Law - 501 pages
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Contents

ADMINISTRATION DEPARTMENT OF HEALTH ANi HUMAN SERVICES
44
Part Page 1 General enforcement regulations 5
50
Product jurisdiction
55
Organization
60
7 Enforcement policy
66
Administrative practices and procedures
76
Electronic records electronic signatures
110
Formal evidentiary public hearing
114
Environmental impact considerations
238
United States and the European Community
250
Protection of human subjects
282
Financial disclosure by clinical investigators
295
Institutional Review Boards
298
Good laboratory practice for nonclinical labora tory studies
308
Patent term restoration
321
Part Page
328

Public hearing before a public board of inquiry
132
Public hearing before a publicadvisory committee
136
Public hearing before the Commissioner
164
Regulatory hearing before the Food and Drug Ad ministration
166
Civil money penalties hearings
172
Standards of conduct and conflicts of interest
188
Public information
191
Protection of privacy
222
Color additive petitions
336
Listing of color additives exempt from certifi
343
Listing of color additives subject to certification
394
Color additive certification L
434
General specifications and general restrictions
440
Listing of certified provisionally listed colors
447
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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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