Standard: HHS - 21 CFR PART 207

REGISTRATION OF PRODUCERS OF DRUGS AND LISTING OF DRUGS IN COMMERCIAL DISTRIBUTION

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Scope:

What is the purpose of this part?

Establishment registration information helps FDA identify who is manufacturing, repacking, relabeling, and salvaging drugs and where those operations are performed. Drug listing information gives FDA a current inventory of drugs manufactured, repacked, relabeled, or salvaged for commercial distribution. Both types of information facilitate implementation and enforcement of the Federal Food, Drug, and Cosmetic Act and are used for many important public health purposes.

Organization: Food and Drug Administration (Medical Products Quality Assurance)
Document Number: 21 cfr part 207
Publish Date: 2017-04-01
Page Count: 16
Change Type: COMPLETE REVISION
Available Languages: EN
DOD Adopted: NO
ANSI Approved: NO
Most Recent Revision: YES
Current Version: YES
Status: Active

Document History

Document # Change Type Update Date Revision Status
21 CFR PART 207 Change Type: COMPLETE REVISION Update Date: 2015-04-01 Status: ACTV
21 CFR PART 207 Change Type: COMPLETE REVISION Update Date: 2014-04-01 Status: ACTV
21 CFR PART 207 Change Type: COMPLETE REVISION Update Date: 2016-04-01 Status: ACTV
21 CFR PART 207 Change Type: COMPLETE REVISION Update Date: 2018-04-01 Status: ACTV

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