About the Conference:

The new stringent European medical device regulations associated with device vigilance system has affected national authorities and economic operators to report serious adverse events that may be associated with a medical device, as well as use errors, product quality issues, and therapeutic failures. These reports, along with data from other sources, can provide critical information that helps improve patient safety.

Addressing medical device vigilance reporting, the two-day conference – 2ndAnnual Medical Device Vigilance Reporting Skills Advancement Conference will focus on guiding and developing industry executives regarding required reporting skills for manufacturers, for user facilities, maintaining complaint files, establishing &maintaining procedures for receiving, reviewing, and evaluating complaints, electronic medical device reporting, developing contracts & agreements etc.

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.Key Speakers:
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