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Webinar Recording: Prepare for EU and Other Global Regulators


RAPS (Regulatory Affairs Professionals Society) hosts as Reed Tech shares their expertise on the topic of ‘Prepare for EU & Other Global Regulators’.  On the agenda:

  • The known requirements of emerging regulatory channels and commercial UDI adopters
  • Best practices in planning for electronic data submissions for UDI
  • The differences and similarities of FDA UDI and EU UDI, touching on device registration scenarios

A short excerpt:

This 60 minute webinar will be beneficial for those in the following roles:

  • Unique Device Identification 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

To see the full presentation, please register. Thanks!


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