Proposed revision to NSF/ANSI 455-4 – Good Manufacturing Practices for Over-the-Counter Drugs (455-4i31r1) The proposed revision will add Section 4.6.19 to ensure laboratory records come into compliance with the FDA and other regulatory authorities.
06911: Approval of 455-4i31r1 - Section 4.6.19
Document (Archive)
2021-04-01
BLANK Comment Template.docx
Document
2021-03-04
gmpOTC-2020-9- Section 4.7.19 (455-4i31).pdf
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