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