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NSF/ANSI 455-4-2022

Good Manufacturing Practices for Over-the-Counter Drugs

standard by NSF/ANSI, 04/01/2023

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About This Item

 

Full Description

This standard is intended to define a standardized approach for auditing to determine the level of compliance of over-the-counter (OTC) drug products to 21 CFR Part 210 and 21 CFR Part 211, International Council for Harmonisation of Technical Requirements for Pharmaceutical for Human Use (ICH) Quality Guidelines, 1, 7 and 10, as well as incorporating additional retailer requirements.

 

Product Details

Published:
04/01/2023
ANSI:
ANSI Approved
Number of Pages:
60
File Size:
1 file , 1.2 MB
Note:
This product is unavailable in Ukraine, Belarus, Russia
 

Document History

  1. NSF/ANSI 455-4-2022

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    Good Manufacturing Practices for Over-the-Counter Drugs

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  2. NSF/ANSI 455-4-2021


    Good Manufacturing Practices for Over-the-Counter Drugs

    • Historical Version

  3. NSF/ANSI 455-4-2020


    Good Manufacturing Practices for Over-the-Counter Drugs

    • Historical Version

  4. NSF/ANSI 455-4-2018


    Good Manufacturing Practices for Over-the-Counter Drugs

    • Historical Version