PART 211—CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
- SUBPART A—General Provisions (§211.1 to §211.3)
- SUBPART B—Organization and Personnel (§211.22 to §211.34)
- SUBPART C—Buildings and Facilities (§211.42 to §211.58)
- SUBPART D—Equipment (§211.63 to §211.72)
- SUBPART E—Control of Components and Drug Product Containers and Closures (§211.80 to §211.94)
- SUBPART F—Production and Process Controls (§211.100 to §211.115)
- SUBPART G—Packaging and Labeling Control (§211.122 to §211.137)
- SUBPART H—Holding and Distribution (§211.142 to §211.150)
- SUBPART I—Laboratory Controls (§211.160 to §211.176)
- SUBPART J—Records and Reports (§211.180 to §211.198)
- SUBPART K—Returned and Salvaged Drug Products (§211.204 to §211.208)