FDA Adverse Event Monitoring and Postmarketing Surveillance for Medical Devices

Nov 27th, 2012Nov 28th, 2012
London, H9
GB
http://www.management-forum.co.uk/medical/eventid/2118
Phone:44 (0) 1483 730071
This course provides a detailed introduction to FDA regulations in the field of medical device safety. The program includes a comprehensive overview of adverse event reporting during research and postmarketing.
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