A Complaint Management Primer: Compliance-Driven Strategies for Effective Complaint Management
Medical device complaint handling and adverse event reporting has been required since the first iterations of ISO 13485 and FDA guidance for quality systems. Yet, complaint management practices continue to be the top reasons for FDA 483 observations and warning letters. This webinar will discuss...
Medical device complaint handling and adverse event reporting has been required since the first iterations of ISO 13485 and FDA guidance for quality systems. Yet, complaint management practices continue to be the top reasons for FDA 483 observations and warning letters. This webinar will discuss strategies for implementing a complaint management process that facilitates gathering, evaluating, investigating and remediating complaints from the premarket stage to closure–and what practices to avoid.
|>Dates and locations:||March 19, 2019 - March 20, 2020|
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