Current Good Manufacturing Practices ― Pharmaceutical, Biologics, and Medical Device Regulations and Guidance Documents: Code of Federal Regulations Title 21: Concise Desk Reference

FDA Regulations and Associated Guidance Documents:- Part 11 Electronic Records; Electronic Signatures- Part 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- Part 200 Drugs General- Part 207 Registration of Producers of Drugs and Listing of Drugs in Commercial Distribution- Part 210 Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs- Part 211 Current Good Manufacturing Practice For Finished Pharmaceuticals- Part 600 Biological Products: General- Part 807 Establishment Registration and Device Listing for Manufacturers and Initial Importers of Devices- Part 820 Quality System RegulationReference Tools:- Glossaries combined in one location- GMP Keyword Index for 21CFR211- Combined Index for all documents