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Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation 2025
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(0 reviews)Thursday, May 5, 2022 (1 day), San Jose, United States
Overview
Date: May 5, 2022 (1 day)
Venue 6201 America Center Drive, San Jose, CA 95002, USA, San Jose, United States
Organizer ComplianceOnline
Attend this webinar to understand, what are the changes to the previous medical device regulation and how to implement the changes in your current quality management system in a simple and quick way. This need smart ideas to reach the right level to pass the quality management audit by your certification company or notified body.
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