Quality Assurance Resources
- Current Good Manufacturing Practices from FDA/CDER
- Human Drug cGMP Notes from FDA/CDER
- cGMPs for Finished Pharmaceuticals Part 820 - Good Manufacturing Practices for Medical Devices
- Proposed revision of cGMP 21 CFR Parts 210 and 211; cGMP; Proposed amendment of certain requirements for finished pharmaceuticals (May 3, 1996)
- 21 CFR Part 110 - cGMP in Manufacturing, Packing, and Handling Human Food