- 21 CFR Part 4 - Current Good Manufacturing Practice Requirements for Combination Products (As of 1 April 2013)
- 21 CFR Part 210 - Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs (As of 1 April 2013)
- 21 CFR Part 211 - Current Good Manufacturing Practice For Finished Pharmaceuticals- (As of 1 April 2013)
Historical preambles announcing changes and comments regarding 21 CFR Parts 210 and 211. - 21 CFR Part 212 Current Good Manufacturing Practice for Positron Emission Tomography Drugs - (As of 1 April 2013)
- 21CFR Part 110 - Current Good Manufacturing Practice in Manufacturing, Packing, or Holding Human Food (As of 1 April 2013)
Historical preambles announcing changes and comments regarding 21 CFR Part 110.
- 21 CFR Part 606 - Current Good Manufacturing Practice For Blood and Blood Components (As of 1 April 2013)
Historical preambles announcing changes and comments regarding 21 CFR Part 606 - 21 CFR Part 820 - Quality System Regulation (As of 1 April 2013)
Historical preambles announcing changes and comments regarding 21 CFR Part 820. - 21 CFR Part 111 - Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements (As of 1 April 2013)
Historical preambles announcing changes and comments regarding 21 CFR Part 111
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