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10 Things You Must Know About Updating Your Technical Files to Comply with EU MDR

This on-demand webinar, hosted by Greenlight Guru, is an essential guide for medical device manufacturers navigating the complexities of complying with the new EU Medical Device Regulation (MDR). Watch this webinar for in-depth insights into the critical changes and expectations for technical documentation under EU MDR. Main points covered: 1. Key changes in technical file requirements under EU MDR. 2. The importance of maintaining technical files as dynamic, living documents. 3. New standards for demonstrating equivalence in technical documentation. 4. Enhanced Quality Management System (QMS) requirements under MDR. 5. Integrating risk management into technical file development and updates. Target Audience: • Medical Device Executives • Regulatory Affairs Professionals and Management • Quality Professionals and Management • Clinical Affairs Professionals and Management • R&D Engineers and Management Access the printable slides for this presentation by visiting: https://www.greenlight.guru/webinar/t...