Date(s) - Tue 14. Dec 2021
8:00 - 16:00
Kategorien Keine Kategorien
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 involves far-reaching changes, including in the classification, clinical testing and quality management of medical devices and in vitro diagnostics.
Together with their partners, Medidee offers an exclusive free check of your situation with regard to the new regulatory requirements, every second Tuesday of a month.
For further information or to book an appointment, please click here.