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2 min reading time
Even though the Corrective and Preventive Action (CAPA) process is at the heart of any quality management system, CAPA violations are the most frequently observed Quality System subsystem cited by FDA.
It happens year after year – and regardless of the devicemaker’s category or size – so I asked resident expert Jon Speer (founder of Greenlight Guru) to co-host a webinar about CAPA.
The online event is free, two weeks from today. Register at https://medgroup.biz/capa and you’ll get the slides even if you can’t attend live.
CAPA implementation and maintenance with yesterday’s systems is hard. Device makers often stumble with poor root cause determination, being reactive instead of proactive, poor definition of a CAPA process, overuse versus underuse and more.
Implementing a robust and modern approach to CAPA will lower your stress level. Well, I think so, anyway. I’d choose preparation over reaction any day.
During this free webinar, you’ll learn:
Who should attend:
Find out for yourself why Jon is consistently rated among our best and most knowledgeable speakers.
As a bonus, all who attend the live event will get a $100 coupon off Jon’s in-person workshop at the 10x Medical Device Conference in April (New Jersey). Learn more at https://medgroup.biz/10x.
And visit https://medgroup.biz/capa now for the December 12 webinar. See you there.
Good group conversation: Will cybersecurity kill med device innovation? at http://bit.ly/cymdv
Make it a great week.
Roger Cepeda, JD, MBA, RAC
Claus Rømer Andersen
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