UDI Product Data and EUDAMED, Get Onboard!

This on-demand webinar hosted by Greenlight Guru focuses on UDI (Unique Device Identification) product data and the European Database on Medical Devices (EUDAMED).
It provides insights into the best practices for preparing for EU EUDAMED, understanding its impact on medical device manufacturers, and the current voluntary activities to engage in.
Main points covered:
1. Overview of the 6 Modules of EUDAMED.
2. Guidance on current voluntary activities and steps to take now.
3. Updated implementation timeline for the In Vitro Diagnostic Regulation (IVDR).
4. Reporting and labeling strategies for UDI data.
5. Solutions to assist with UDI data requirements and EUDAMED compliance.
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 here:
www.greenlight.guru/webinar/u...