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.
bag
fda_public
created
Sun, 01 Jul 2012 15:05:22 GMT
creator
dirkjan
modified
Sun, 01 Jul 2012 15:05:22 GMT
modifier
dirkjan
tags
CFR 21-820.30
Design Controls
FDA
Quality System Requirements
Term
creator
dirkjan