Proposed revision to NSF/ANSI 455-2 – Good Manufacturing Practices for Dietary Supplements (455-2i30r1) The purpose of this issue paper is to add a serious adverse event reporting procedure requirement.
07621: Approval of 455-2i30r1 - Sec 4.6.18 Serious Adverse Events
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2022-05-20
gmpDS-2021-20 - Sec 4.6.18 Serious Adverse Events.pdf
Document
2022-04-27
Blank Comment - TEMPLATE.docx
455-2i30 - 2021 GMP-DS JC Meeting Summary Excerpt.pdf
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