Managing Your Medical Device Reporting (MDR)Program for Compliance Success - Webinar By GlobalCompliancePanel

13 March 2013, Fremont, United States

Introduction

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.

Price: $225.00

GlobalCompliancePanel
Phone: 800-447-9407
webinars@globalcompliancepanel.com

http://bit.ly/QrDZVM