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Talk:Contract development and manufacturing organisation

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This article is within the scope of the quality and testing working group.

This is the discussion page for the article Contract development and manufacturing organisation. 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.

Not inherently suspiciousResolved

Community discussion often treats contract manufacture as though it were concealment. It is the normal structure of the industry and the article says so plainly. CDMO_Caradoc (talk) 09:45, 22 January 2026 (UTC)

Including for approved medicines, which is the comparison that settles it. ✓ Done GMP_Gita (talk) 13:20, 22 January 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.

Checkable claimsDone

"A specific claim about a facility, a certification or a capability is a checkable claim; a general impression conveyed by photographs and adjectives is not" — that is the criterion the supplier articles use and it is good to have it stated somewhere. VerifyVesna (talk) 10:30, 14 April 2026 (UTC)

It belongs here rather than on any individual supplier article, where it would read as pointed. ✓ Done DisclosureDido (talk) 14:05, 14 April 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 14 April 2026, by DisclosureDido. Text is available under the PeptidePedia Wiki Content Licence (PPCL-BY-SA 4.0).