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Regulations last checked for updates: May 20, 2024
Title 21 - Food and Drugs last revised: May 15, 2024
All Titles
Title 21
Chapter I
Part 111 - PART 111—CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
Subpart A [§ 111.1 - § 111.5] - Subpart A—General Provisions
Subpart B [§ 111.8 - § 111.14] - Subpart B—Personnel
Subpart C [§ 111.15 - § 111.23] - Subpart C—Physical Plant and Grounds
Subpart D [§ 111.25 - § 111.35] - Subpart D—Equipment and Utensils
Subpart E [§ 111.55 - § 111.95] - Subpart E—Requirement to Establish a Production and Process Control System
Subpart F [§ 111.103 - § 111.140] - Subpart F—Production and Process Control System: Requirements for Quality Control
Subpart G [§ 111.153 - § 111.180] - Subpart G—Production and Process Control System: Requirements for Components, Packaging, and Labels and for Product That You Receive for Packaging or Labeling as a Dietary Supplement
Subpart H [§ 111.205 - § 111.210] - Subpart H—Production and Process Control System: Requirements for the Master Manufacturing Record
Subpart I [§ 111.255 - § 111.260] - Subpart I—Production and Process Control System: Requirements for the Batch Production Record
Subpart J [§ 111.303 - § 111.325] - Subpart J—Production and Process Control System: Requirements for Laboratory Operations
Subpart K [§ 111.353 - § 111.375] - Subpart K—Production and Process Control System: Requirements for Manufacturing Operations
Subpart L [§ 111.403 - § 111.430] - Subpart L—Production and Process Control System: Requirements for Packaging and Labeling Operations
Subpart M [§ 111.453 - § 111.475] - Subpart M—Holding and Distributing
Subpart N [§ 111.503 - § 111.535] - Subpart N—Returned Dietary Supplements
Subpart O [§ 111.553 - § 111.570] - Subpart O—Product Complaints
Subpart P [§ 111.605 - § 111.610] - Subpart P—Records and Recordkeeping
authority:
21 U.S.C. 321
,
342
,
343
,
371
,
374
,
381
,
393
;
42 U.S.C. 264.
source:
72 FR 34942, June 25, 2007, unless otherwise noted.
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