Using Quality and Risk as Tools, not Hurdles

PODCAST
Written By Christie Johnson
 

Do you come from a development background but are leaping into new waters with medical devices?

This podcast is recorded for you and provides a great overview of quality, product development processes, design controls, managing risk, and the importance of documentation in this unique industry.

Christie Johnson speaks with Grant Chapman and Ben Ettinger in episode 14 of the Glasslab Podcast and it’s full of great advice plus a few good laughs.

 
 
Christie Johnson
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Intersection of ISO 13485 and ISO 14971 under FDA QMSR
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Project Management for Product Development of Medical Devices