Part 211 — Current Good Manufacturing Practice for Finished Pharmaceuticals
- Subpt. A General Provisions §§211.1 to 211.3
- Subpt. B Organization and Personnel §§211.22 to 211.34
- Subpt. C Buildings and Facilities §§211.42 to 211.58
- Subpt. D Equipment §§211.63 to 211.72
- Subpt. E Control of Components and Drug Product Containers and Closures §§211.80 to 211.94
- Subpt. F Production and Process Controls §§211.100 to 211.115
- Subpt. G Packaging and Labeling Control §§211.122 to 211.137
- Subpt. H Holding and Distribution §§211.142 to 211.150
- Subpt. I Laboratory Controls §§211.160 to 211.176
- Subpt. J Records and Reports §§211.180 to 211.198
- Subpt. K Returned and Salvaged Drug Products §§211.204 to 211.208