WEBINAR: ISO13485: 2016 – An Overview of General and Product Realisation Requirements
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In 15 minutes, ascertain the major changes to the new ISO 13485: - Impacts of the new revision - New terminology - General requirements - Resource management - Product realisation and design controls - Q&A session Led by Richard Young, trainer for MDTI's Managing the Transition to the new IVD Regulation and Practical Guidance for Medical Device ...
3.5K viewsNov 18, 2016
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