On 26th May 2021 the new Medical Device Regulation (MDR) 2017/745 has entered into force !
From this date, only Medical Devices that are compliant with the new MDR should continue to be marketed in the European Market.
If you still do not comply, it is urgent to start the compliance process to be able to continue to sell your devices.
Come to discover with us how to be compliant with the MDR 2017/745 !
During this webinar, we will answer the following questions :
After more than 6 years of experience as a sales representative in long sales cycles, and a double technical-commercial competence, Raïssa supports manufacturers in the compliance of their medical devices.