Life Sciences Blog

Webinar Recording: EU MDR-Best Practices for UDI Data & Product Labeling

by | Jan 22, 2020

In this free webinar, featured speakers from Reed Tech and PRISYM ID discuss what device companies will need to do to be EU MDR compliant.

Who will benefit?

This webinar will be suitable for individuals with the following or related job titles:

  • Unique Device Identification (UDI) Team Members
  • Product Labeling Team Members
  • Global Strategy Business Managers
  • Regulatory Affairs/Operation Leaders
  • Product Managers and Business Analysts
  • Manufacturing, Operations, and Supply Chain Leaders
  • Quality Leaders
  • Medical Device IT Support Personnel

To view the full recording, click on the image below. Thank You!

Global UDI Summary - Download Fact Sheet

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