Regulatory Check-Up: 1 Stunde kostenfreie Beratung

Since May 2021, the new EU Medical Devices Regulation ((EU) 2017/745 Regulation on medical devices (MDR)) has come into force, and from May 2022, the new EU In-vitro Diagnostics Regulation ((EU) 2017/746 Regulation on in-vitro diagnostic medical devices (IVDR)) will follow it.

This will be accompanied by far-reaching changes, including in the classification, clinical testing and quality management of medical devices and in vitro diagnostics.

Together with our partners, we offer you an exclusive free check of your situation with regard to the new regulatory requirements.

Registration

Are all appointment options already taken? Please contact us at the following e-mail address to arrange additional appointments and options: raimo.sump@medidee.com