In FDA [[Design Controls|CFR 21-820.30 - Design Controls]] the ''//Medical Device Report//'' (MDR) means Medical Device Reporting. To be elaborated...
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fda_public
created
Sun, 01 Jul 2012 19:09:50 GMT
creator
dirkjan
modified
Sun, 01 Jul 2012 19:09:50 GMT
modifier
dirkjan
tags
CFR 21-820.30
Design Controls
FDA
Quality System Requirements
Term
creator
dirkjan