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Managing Your Medical Device Reporting (MDR)Program for Compliance Success

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Managing Your Medical Device Reporting (MDR)Program for Compliance Success

Published on Feb 4, 2013

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Medical Device Reporting (MDR) is the mechanism for the Food and Drug Administration to receive significant medical device adverse events from manufacturers, importers and user facilities, so they can be detected and corrected quickly. If you are a consumer or health professional you should use the MEDWATCH program for reporting significant adverse events or product problems with medical products.

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