RESOURCES / WHITEPAPERS

THE IVDR TOP 8 - A Roadmap For Transitioning To The European in vitro Diagnostic Medical Devices Regulation (IVDR)

THE TIME FOR ACTION IS NOW. GET YOUR ROADMAP FOR IVDR COMPLIANCE.

 

Notified Body (NB) representatives have been quoted calling EU IVDR the “big bomb” and are advising IVD industry that if they haven’t started already, they may already be too late to meet the deadline for EU IVDR implementation on May 26, 2022.

  • No grandfathering of IVD products currently on the market
  • No grace period for self-certified products under prior IVD Directive
  • A solid strategy is key
  • Network Partners is your ally in IVDR compliance

 

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