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HHS - 21 CFR PART 210

CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL

active, Most Current
Organization: HHS
Publication Date: 1 April 2017
Status: active
Page Count: 4

Document History

21 CFR PART 210
April 1, 2022
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL
A description is not available for this item.
21 CFR PART 210
April 1, 2021
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL
A description is not available for this item.
21 CFR PART 210
April 1, 2019
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL
A description is not available for this item.
21 CFR PART 210
April 1, 2018
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL
Applicability of current good manufacturing practice regulations. (a) The regulations in this part and in parts 211, 225, and 226 of this chapter as they may pertain to a drug; in parts 600 through...
21 CFR PART 210
April 1, 2017
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL
A description is not available for this item.
21 CFR PART 210
April 1, 2016
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL
Applicability of current good manufacturing practice regulations. (a) The regulations in this part and in parts 211, 225, and 226 of this chapter as they may pertain to a drug; in parts 600 through...
21 CFR PART 210
April 1, 2015
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL
Applicability of current good manufacturing practice regulations. (a) The regulations in this part and in parts 211, 225, and 226 of this chapter as they may pertain to a drug; in parts 600 through...
21 CFR PART 210
April 1, 2014
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL
A description is not available for this item.
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References

This document is referenced by:
TR 12417-2 - Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 2: Local regulatory information
Published by ISO on July 1, 2022
This document provides region-specific information for: — local submissions and approvals for vascular device-drug combination products (VDDCPs) in countries and regions around the world; — changes...
This document is referenced by:
NFPA MGHB - Medical Gas and Vacuum Systems Handbook
Published by NFPA on January 1, 2021
A description is not available for this item.
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