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Medical Device Complaints, MDRs & Reports Workshop
3/13/2018

April 4-5 | Washington, D.C.
How do you implement and measure the effectiveness of a complaint-handling system covering a diverse set of possible products and problems? How are complaint files managed across multiple domestic and international facilities? When do complaints rise to the level of MDRs, and how do you handle recalls? What are the current FDA enforcement trends in these areas? Industry experts and FDA staff will explore these issues during this two-day workshop. Learn more.

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