In FDA [[Design Controls|CFR 21-820.30 - Design Controls]] the ''//Master Verification//'' or Validation Plan is a document that identifies all responsibilities, expectations, systems and subsystems involved with a specific verification or validation activitity and the qualification approaches that ensure verification or total system validation.
bag
fda_public
created
Sun, 01 Jul 2012 19:21:21 GMT
creator
dirkjan
modified
Sun, 01 Jul 2012 19:21:21 GMT
modifier
dirkjan
tags
CFR 21-820.30
Design Controls
FDA
Quality System Requirements
Term
creator
dirkjan