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.


Christophe Amiel, Senior Director Medical Devices & Digital Life Sciences

Christophe Amiel is heading the design and implementation of regulatory strategy as Senior Director within Voisin Consulting Life Sciences for medical devices (including in vitro diagnostics), digital life sciences, as well as combination products (drug-device association) including activities related to Clinical Trials Application and vigilance.

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