EAS Webinar: FDA’s Transition from CFR 820 to the ISO 13485

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	George Yanulis Fort Myers, FL	EAS Webinar: FDA’s Transition from CFR 820 to the ISO 13485
	Website - Blog - Twitter	Posted by George Yanulis on 10.08.19 in Miscellaneous
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Dr. Yanulis is an experienced medical device research and development engineer and medical device expert witness.		EAS Webinar: FDA’s Transition from CFR 820 to the ISO 13485:2016 - Instituting a New Quality Management System (QMS) September 25, 2019 Presented by George Yanulis, D.Eng., EAS Independent Consultant FDA’s shift ...