This offer is available every second Tuesday of a month
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.
Medidee offers you an exclusive free check of your situation with regard to the new regulatory requirements.
Medical device and in vitro diagnostic companies can sign up for one of the monthly appointments by using this webpage: Regulatory Check Up – Medidee Services