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HomeU.S. FDA Guidance › Code of Federal Regulations

Code of Federal Regulations: 21 CFR Part 11 (U.S. FDA)


The Code of Federal Regulations (CFR) is the codification of the general and permanent rules published in the Federal Register by the executive departments and agencies of the Federal Government. It is divided into 50 titles that represent broad areas subject to Federal regulation. Each volume of the CFR is updated once each calendar year and is issued on a quarterly basis.

Food and Beverages Regulations
Medical Devices Regulations
  • 21 CFR Part 11 U.S. FDA Medical Device Establishment Registration and Device Listing Regulations
  • 21 CFR Part 11 U.S. FDA Medical Device Labeling Regulations
Cosmetics Regulations
  • 21 CFR Part 11 U.S. FDA Voluntary Cosmetic Registration Program
  • 21 CFR Part 11 U.S. FDA Cosmetics Labeling Regulations
Drugs Regulations




 









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