P
pheuvelmans
What results of a design review are documented in a DHF, as they shall be used in medical device industry, to be FDA compliant?
Should all comments, issues which are made by the reviewers, be documented, or is the modified and committed / approved document, which is reviewed, sufficient?
Who can help me out?
Should all comments, issues which are made by the reviewers, be documented, or is the modified and committed / approved document, which is reviewed, sufficient?
Who can help me out?