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HHS - 21 CFR PART 111

CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS

active, Most Current
Organization: HHS
Publication Date: 1 April 2021
Status: active
Page Count: 31

Document History

21 CFR PART 111
April 1, 2023
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
A description is not available for this item.
21 CFR PART 111
April 1, 2022
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
A description is not available for this item.
21 CFR PART 111
April 1, 2021
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
A description is not available for this item.
21 CFR PART 111
April 1, 2020
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
A description is not available for this item.
21 CFR PART 111
April 1, 2019
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
A description is not available for this item.
21 CFR PART 111
April 1, 2017
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
A description is not available for this item.
21 CFR PART 111
April 1, 2016
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
A description is not available for this item.
21 CFR PART 111
April 1, 2015
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
Who is subject to this part? (a) Except as provided by paragraph (b) of this section, you are subject to this part if you manufacture, package, label, or hold a dietary supplement, including: (1) A...
21 CFR PART 111
April 1, 2014
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
Who is subject to this part? (a) Except as provided by paragraph (b) of this section, you are subject to this part if you manufacture, package, label, or hold a dietary supplement, including: (1) A...
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References

This document is referenced by:
NSF 455-2 - Good Manufacturing Practices for Dietary Supplements
Published by NSF on April 6, 2020
This Standard is intended to define a standardized approach for auditing to determine the level of compliance of dietary supplement products to 21 CFR Part 111, Current Good Manufacturing Practices...
This document is referenced by:
NSF 14 - Plastics Piping System Components and Related Materials
Published by NSF on June 22, 2020
The physical, performance, and health effects requirements in this Standard apply to thermoplastic and thermoset plastic piping system components including, but not limited to, pipes, fittings,...
This document is referenced by:
C22.2 NO. 60601-1-2:16 - Medical electrical equipment — Part 1-2: General requirements for basic safety and essential performance — Collateral Standard: Electromagnetic disturbances — Requirements and tests
Published by CSA on January 1, 2016
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS....
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