This on-demand webinar hosted by Greenlight Guru explains how to comply with the new European Union Medical Device Regulation (EU MDR). This webinar is essential for medical device professionals looking to navigate the complexities of the EU MDR.

Main points covered:
1. Key dates, timelines, and limitations related to the EU MDR.
2. Impact of the regulations on QMS processes and their relation to EU MDR and ISO 13485:2016.
3. Workflow processes for conformity assessments of medical devices.
4. Essential steps for compliance with the new regulations.
5. Strategies for transition based on industry experiences.

Target Audience:
• Medical Device Executives
• Regulatory Affairs Professionals
• Quality Management Professionals
• Clinical Affairs Professionals
• R&D Engineers

Access the printable slides for this presentation here:
[ Ссылка ]

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