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IVD Regulatory and Strategic Forum

Get ready for the move to the IVDR

The IVD industry is about to change

Delve into the details of the IVDR
  • Implementing the IVDR – Competent Authority, Notified Body and industry perspectives
  • Understanding the implications of the new clinical evidence requirements
  • Do you understand the responsibilities of the Person Responsible for Regulatory Compliance?
  • How will PMS and vigilance requirements change under the IVDR?
  • What challenges is the IVDR creating for companion diagnostics manufacturers?
Competent Authority and Notified Body perspectives from:

MHRA
LRQA
UL
DEKRA

Join the discussion

Our interactive sessions will allow you to:

  • Discuss how to implement the IVDR with the MHRA, LRQA, UL, and industry
  • Share experiences with increased clinical data requirements
  • Understand how the companion diagnostics industry should be preparing for the IVDR