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Regulations last checked for updates: May 22, 2025

Title 21 - Food and Drugs last revised: May 19, 2025
All TitlesTitle 21Chapter IPart 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
authority: 21 U.S.C. 321,351,352,355,360b,371,374; 42 U.S.C. 216,262,263a,264
source: 43 FR 45077, Sept. 29, 1978, unless otherwise noted.
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