About this event
With this webinar, get insights on the regulatory framework in the EU regarding Medical Devices and Digital Therapeutics.
You will receive information on:
- Regulatory Classifications
- CE marking requirements
- How to build your roadmap?
Hosted by
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Guest speaker
Christophe Amiel Senior Director, Medical Devices & Digital Life Sciences @ Voisin Consulting Life SciencesG
Christophe is heading design and implementation of regulatory strategy for medical devices (incl. software as component or as standalone product), combo (drug, biologic) & borderline products. His areas of expertise encompass product design/validation, clinical development and international market approvals. As Head of Activity he is also responsible for the development of MedTech activities (incl. market intelligence, experts networking, etc.)
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Guest speaker
Sébastien Giraudier Director @ Neighbhorhood, VCLS Innovation CenterG
Sébastien leads Neighborhood the VCLS’s innovation center. Neighborhood supports health tech entrepreneurs providing strategic mentorship and resources, experts and office space for growth and build their development strategies.
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Team member
Yann Masson HealthTech & Life Sciences expert @ Choose Paris RegionT
Yann is the Healthtech & Life Sciences expert at Choose Paris Region. He is guiding daily HealthTech companies looking to explore the large ecosystem of the Paris Region.
Choose Paris Region
Come for the business, stay for life!Set up and scale up your business in Paris Region, main hub of the European market, to expand your international business.
