How and When to Register EU Medical Devices and Report UDI Information to EUDAMED

This on-demand webinar, hosted by Greenlight Guru, offers a comprehensive guide on the process and requirements for registering medical devices in the EU and reporting UDI information to the EUDAMED database.

Follow along as we take a look at UDI data elements, review key differences of UDI between FDA and EU, and cover advantages of a central product information management solution to prepare you in defining your UDI roadmap.

Main points covered:
1. The requirements for registering medical devices and reporting UDI to the EU EUDAMED database.
2. The step-by-step process of registering EU medical devices and reporting to EUDAMED.
3. Comparisons between FDA UDI (GUDID) and EU UDI (EUDAMED) requirements.
4. The benefits of a comprehensive, global strategy for UDI compliance.
5. Q&A session addressing specific concerns and queries.

Target Audience:
• UDI Team Members
• Global Strategy Business Managers
• Regulatory Affairs/Operation Leaders
• Product Managers and Business Analysts
• Manufacturing, Operations, and Supply Chain Leaders
• Quality Leaders

Access the printable slides for this presentation by visiting:
https://www.greenlight.guru/webinar/h...