Design Master Record

From knowledgebase

Revision as of 07:19, 25 August 2020 by Dirkjan (talk | contribs) (Created page with "In the FDA's Quality System Requirements the ''Design Master Record'' (DMR) means a compilation of records containting the procedures and specifications for a finished device....")

(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

Jump to navigation Jump to search

In the FDA's Quality System Requirements the Design Master Record (DMR) means a compilation of records containting the procedures and specifications for a finished device.

Retrieved from "https://wiki.dirkjanswagerman.nl/index.php?title=Design_Master_Record&oldid=547"