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On-Demand Webinar

The first significant changes to medical device regulations in the European Union (EU) in over 25 years will start to go into effect in less than 3 years. Among the many changes is the introduction of a UDI System for all medical devices – are you ready? Join us and find out.

The discussion will include:
  • An exploration of the similarities and differences between the US and EU UDI requirements
  • Important implementation issues
  • What to expect from other countries as UDI becomes a global practice
  • Live Q & A session
About the Presenter:

Jay Crowley

Vice President of Unique Device Identification Jay was Senior Advisor for Patient Safety in the Food and Drug Administration’s Center for Devices and Radiological Health. Jay developed the framework and authored key requirements for the FDA’s Unique Device Identification system.

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