In FDA [[Design Controls|CFR 21-820.30 - Design Controls]] the ''//Master Verification//'' are documented functions, conditions, or capabilities that a medical device must meet or possess to satisfy a user's need, standard or regulatory expectations.
bag
fda_public
created
Sun, 01 Jul 2012 19:12:56 GMT
creator
dirkjan
modified
Sun, 01 Jul 2012 19:12:56 GMT
modifier
dirkjan
tags
CFR 21-820.30
Design Controls
FDA
Quality System Requirements
Term
creator
dirkjan