This on-demand webinar, hosted by Greenlight Guru, focuses on effective strategies for preparing technical documentation in compliance with the EU Medical Device Regulation (MDR). Learn about the latest EU updates, including regulation 2023/607 and MDCG guidance documents, and practical tips and techniques for MDR compliance.
Main points covered:
1. Understanding current requirements under EU MDR.
2. Utilizing available tools for industry compliance.
3. Strategies for clear communication with Notified Bodies.
4. Key focus areas in technical documentation and Quality Management Systems (QMS) under MDR.
5. Approaches taken by Notified Bodies during the CE certification process.
Target Audience:
• Regulatory Affairs Professionals & Management
• Quality Professionals and Management
• Medical Device Executives
• Product Development Engineers and Management
Access the printable slides for this presentation by visiting:
www.greenlight...