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  1. Regulations
    All Titles
  2. title 21
    Food and Drugs
  3. chapter I-i3
    CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)
  4. part 211
    PART 211—CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS

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
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