Code of Federal Regulations > Title 21 > Chapter I > Part 111 - PART 111—CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS

U.S. Code of Federal Regulations

Regulations most recently checked for updates: Sep 14, 2024

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