Code of Federal Regulations > Title 21 > Chapter I > Part 211 - PART 211—CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS

U.S. Code of Federal Regulations

Regulations most recently checked for updates: Jan 18, 2025

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