Medical Devices placed on the market must be compliant with the regulation 2017/745 in force. The compliance process requires a huge investment of resources, time, energy etc.
To be well prepared, you must organize your team budget and project in order to successfully register your products within the obligations and your launching timelines.
During this webinar, we will explain the different steps of the compliance process and give you the tips to anticipate the critical points (documentation, standards, financial, human, time resources etc).
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.