In vitro diagnostic medical devices (IVD) are tests performed on human samples (such as blood, urine or tissues) to provide information on a person’s health. Until 2017 IVDs were regulated by the Directive 98/79/EC on in vitro diagnostic medical devices (IVDD). In May 2017 the new Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR) came into force.

The IVDD-to-IVDR transition period will end in May 2022. Get ready for the upcoming changes by attending our webinar!

Dr. Solveigh Krusekopf is Senior Consultant in the Consulting & Strategic Innovation team at analyze & realize.

Register now for free!