Medical Device Reporting for Manufacturers – Best Practices to Follow

  • By: Staff Editor
  • Date: December 02, 2011
Webinar All Access Pass Subscription Abstract:

The FDA requires medical device manufacturers to submit reports in case of device malfunctioning. But when and how are these reports to be submitted? Which medical device malfunctions require reporting to the FDA?

This article describes the best practices that medical device manufacturers can follow in order to comply with medical device reporting to the FDA.

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