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Development and Registration of m-Health Technologies for the EU Market

Post thumbnail Development and Registration of m-Health Technologies for the EU Market

e-health technologies are already today starting to revolutionize the therapeutic processes and patients management paradigm. Unfortunately, e-health developers are very often uncomfortable with the regulatory maze they have to navigate into (or are simply unaware of it) until their e-health products could be placed on the European market.

Key learning objectives:

  • European regulatory framework applicable to m-health technologies
  • m-health products development and evaluation
  • Critical regulatory challenges for the EU market

Christophe Amiel, Senior Director at VCLS, will share his experience on these innovative m-health technologies and the associated development hurdles. He will illustrate critical matters related to the regulatory environment relevant to e-health products and how to best overcome these challenges for derisking market launch in Europe.

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    Featured Speakers

    Christophe Amiel
    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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