Greenlight Guru hosts as Reed Tech shares their expertise on the topic of ‘Registering EU Medical Devices and Reporting UDI info to EUDAMED’.
A short excerpt:
In this 60-minute webinar, you’ll learn:
- How and when to register EU medical devices and report UDI information to EUDAMED
- Expected future challenges in implementing UDI
- Key differences of UDI between FDA and EU EUDAMED (some of which may surprise you)
- Lastly, we will cover advantages of a central product information management solution to prepare you in defining your UDI roadmap
This webinar was hosted by Greenlight Guru. The only Quality Management Software designed speciﬁcally for the medical device industry.