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Podcast: Compliance 360° Part 14 – Leverage FDA Data To Stay In The Agency's Good Graces

 
• By Shawn M. Schmitt

This is Compliance 360°, a podcast series from Medtech Insight on US FDA compliance and enforcement issues. In this fourteenth installment, former FDA investigations branch director Ricki Chase explains how device-makers can leverage publicly available data from the agency to determine where they might fall short when it comes to complying with FDA rules and regulations.

MT1701_Compliance360

Device-makers should leverage US FDA's publicly available information on facility inspection observations, adverse events, recalls and other data to determine where they might fall short when it comes to complying with agency rules and regulations. That's the message from former US FDA investigations branch director Ricki Chase in this 14th installment of Compliance 360°, a podcast series from Medtech Insight on FDA compliance and enforcement issues.

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