Dirkjan: 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...."

2020-08-25T07:19:15Z

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...."

New page

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.
[[Category:fda]]

[[Category:CFR 21-820.30]]

[[Category:Design Controls]]

[[Category:FDA]]

[[Category:Quality System Requirements]]

[[Category:Term]]

Design Master Record - Revision history

Dirkjan: 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...."