Copan is ready for the new #MDR and #IVDR regulations

Copan have worked relentlessly in the last four years to comply with applicable MDR and IVDR requirements. And now they are ready!

May 26, 2022, was the outset of IVDR regulations, which set new standards for the quality and safety of in vitro medical devices. Together with MDR, the new regulations impact all the stakeholders of the #healthcare environment, from the manufacturing industries to doctors, practitioners, and laboratorists that need to comply with MDR/IVDR in their daily activities.
As a result, their product regulatory #compliance and supply reliability are guaranteed, ensuring our trusted partners and clients no product family disruption throughout this transition period.

How Copan is facing the EU IVDR Regulation

How Copan is facing the EU MDR Regulation


Please don´t hesitate to contact us if you have any questions.