This webinar helps developers of e-health/m-health solutions to better understand the regulatory environment relevant to their digital technologies in Europe and in the US and how to best overcome these challenges to maximize the chances of a timely and successful market launch on these markets. This webinar outlines how e-health/m-health companies can implement strategic development plan for their products with the aim to minimize the risks and to avoid the introduction of extra delays for reaching the EU and US markets. Opportunities and cautions for placing on these markets such as innovative AI-based and other digital solutions will be shared.
Key topics include:
- EU/US regulatory frameworks applicable to e-health/m-health technologies
- e-health/m-health product development and evaluation under Medical Device scheme
- Critical challenges for placing e-health/m-health solutions on the market in the EU and the US
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Sample of the webinar
Featured Speakers
Christophe Amiel, M.Sc.
Senior Director, Medical Devices & Digital Life Sciences
As a Senior Director at VCLS, Christophe is responsible for leading the Medical Device and Digital Life Science Group. The…
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