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Medical Device Reporting System Software Available In Congo Democratic Republic Of The

1 software items found
RegScan - Version MDR - Medical Device Reporting System

RegScan - Version MDR - Medical Device Reporting System

by:RegScan - by Enhesa   based inWilliamsport, PENNSYLVANIA (USA)
The medical device reporting (MDR) requirements of 21 CFR 803 apply to manufacturers, importers, distributers, and device user facilities in the United States. Such facilities are required to report adverse device-related events to the Food and Drug Administration (FDA) or the ...
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