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Talk:ISO 9001

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This article is within the scope of the regulation working group.

This is the discussion page for the article ISO 9001. It is for improving the article: sources, wording, structure, scope and titles. It is not a general discussion forum about the subject, and it is not a place to ask for advice — see Project:Medical disclaimer.

Scope is on the certificateResolved

Scope is the most informative field and the one people never read. A certificate covering sales and distribution is not a manufacturing claim. — GMP_Gita (talk) 09:45, 19 February 2026 (UTC)

Added to the four-element table so a reader knows what to look for. ✓ Done — VerifyVesna (talk) 13:20, 19 February 2026 (UTC)

Resolved. This thread is closed. Reopening it is fine if new sources appear; please add a new subsection rather than editing the closed discussion.

Accredited versus unaccredited bodiesDone

Worth noting that certificates are also issued by unaccredited bodies, since the distinction determines whether verification is possible. — DMF_Dermot (talk) 10:15, 24 May 2026 (UTC)

Stated with the register route to verification, which is the practical consequence. ✓ Done — GMP_Gita (talk) 13:50, 24 May 2026 (UTC)

Done. This thread is closed. Reopening it is fine if new sources appear; please add a new subsection rather than editing the closed discussion.
This page was last edited on 24 May 2026, by GMP_Gita. Text is available under the PeptidePedia Wiki Content Licence (PPCL-BY-SA 4.0).