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Evolution of the European Regulatory Framework for Innovation – Key Topics for the Future

Post thumbnail Evolution of the European Regulatory Framework for Innovation – Key Topics for the Future

DIA Europe 2019 was held this year in Vienna, Austria. Speakers included national regulators, together with representatives from health technology assessment (HTA) bodies, patient advocacy groups, and other critical stakeholders. Presentations covered the entire healthcare value chain, ranging from policy and regulations to research and development, marketing and access.

In this report, focus will be given to presentations addressing the evolution of the European regulatory framework to support continued innovation. This covers the development of novel medicinal products, devices, diagnostics, together with the application of real world data (RWD) to ensure patients benefit from the potential these technologies offer.

In the opening session, four priorities were identified, and as these are applicable for all stakeholders, they will be discussed in more detail.

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publication by

Chris Wilson
Chris Wilson, B.Sc., M.Sc., MTOPRA
Senior Director, Drugs & Biologics
As Senior Director Regulatory Science, Drugs and Biologics Chris provides leadership and support across Market Access, Regulatory and Medical / Regulatory Writing functions.   In addition to…
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