SUCCESSFULLY LAUNCH YOUR PRODUCTS
ACCORDING TO THE EU MEDICAL DEVICE REGULATION
MEDICAL DEVICES
The medical device market is today regulated by European directives.
As the demand for safety and efficiency is constantly increasing, the EU Medical Device Regulation (MDR) came into force in May 2017.
The new MDR will begin to apply on 26th May 2021 and features several significant changes.
As placing medical devices on the European market is a complex process, we will present you everything you need to know and will show you concrete examples applicable to your business.
What are the main requirements of the new MDR?
How to successfully launch your product and bring it into compliance with the new MDR?
What are the risks if we do not comply with the new regulations?
Why you need to get started as soon as possible?
AGENDA
- Presentation of the new MDR: regulatory constraints and requirements,
- How to comply with the new MDR and what are the risks involved if non-compliance?
- Some examples of successful launches of medical device
REGISTER NOW TO SEE OUR REPLAY!
Raïssa ABDEL-KADER
Business Developer
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.
Morgane MONDON
Regulatory Expert - Cosmetics
Morgane holds a Master's degree from Polytech Nice Sophia engineering school and joined EcoMundo in Paris to bring her expertise in regulatory cosmetic projects, after which she joined our Canadian subsidiary in Montréal.
© EcoMundo 2020
