Following the 1st January 2021, the United Kingdom (UK) will officially leave the European Union and the European Medical Device Regulation 2017/745 will no longer be applied.
The entry into force of Brexit will have consequences for players in the Medical Device sector and the marketing of their products.
From this date, you will need to follow the specific requirements to comply with the UK regulations.
To continue to sell your Medical Device in the UK, it is therefore important to understand now what are the main issues and impacts on your products.
The aim of this webinar is to explain to you the main changes and requirements so to help you to be compliant to the UK regulations.
After 6 years of experience as a sales representative with a good knowledge of long sales cycles, and a double technical-commercial skill, Raïssa joins EcoMundo in Paris in 2020.
Cosmetics Regulatory Expert
Graduate of the Ecole Nationale Supérieure de Chimie de Lille, Agathe started her career at Stanhome as a Project Manager before joining the teams of the Rocher Group as Regulatory Affairs Manager. In 2018, she joined the EcoMundo teams as Cosmetics Director.