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Master Drug and Medical Device Reporting (MDRs)

20 May 2014, Fremont, United States


Introduction
Manufacturers of APIs, Final Drug Products and Medical Devices are required to report to the FDA when they learn that any of their products may have caused or contributed to a death or serious injury or if there is an anticipated patient risk.
Venue
Online Event

Online Event, 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA, Fremont, 94539, United States

Organised by
GlobalCompliancePanel
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