This site uses modern web standards that aren't supported by your browser. For best results, please upgrade to Google Chrome, Microsoft Edge, or Mozilla Firefox.

Webinar Recording: Registering EU Medical Devices & Reporting UDI Info to EUDAMED

|

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

EUDAMED UDI Reed Tech

Play Full Recording

This webinar was hosted by Greenlight Guru. The only Quality Management Software designed specifically for the medical device industry.

By continuing to use the site, you agree to the use of cookies. more information

The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.

Close