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.
EUDAMED is one of the major steps to take into consideration if you would like to be sure to meet the requirements.
Authorities have implemented the new Actor registration module since December 2020.
Come to discover with us the key points of the registration process on the EUDAMED portal !
Cosmetics Director of EcoMundo, Agathe is a graduate of the Ecole Nationale Supérieure de Chimie de Lille. She started her career as a project manager before joining the teams of a large cosmetics group as a regulatory affairs manager.
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.