Carenity invites you to their event

Implementing a DCT - Decentralized Clinical Trial: the road to success

About this event

How to leverage both patient centricity and digital innovation in clinical research?

Over the past years, clinical research has entered a new area with an increasing adoption of DCT – Decentralized Clinical trial – fully or hybrid, which has been accelerated by the COVID-19 pandemic. Thanks to digital health solutions and the recent evolution of regulatory framework, DCT means a promising future for clinical trials. However, there are still challenges to define a DCT strategy for clinical trials.

What are the key success factors to implement a DCT? How to assess what protocol evaluations can be off-site? What are expectations from regulators and IRB/Ethics Committees? How to leverage patient insights to build adapted and patient-centric DCT? How to select the adequate technology components?

Come join us, we will walk you through the key steps to successfully implement a DCT and share EvidentIQ’s expertise and state-of-the-art technologies to support your DCT approach.

Don’t hesitate, register now!

Hosted by

  • Team member
    Thomas Verjus Global Business Development - RWE @ EvidentIQ

    Thomas Verjus is managing global business development activities for EvidentIQ, supporting our life sciences industry and academic partners in RWE and Clinical Trials Optimization projects. Thomas has more than 10 years of international experience in the life sciences industry.

  • Team member
    Thierry Escudier Strategic Consultant @ DCRIPT

    Thierry Escudier is a leader in Clinical Research, with more than 30 years experience in Corporate R&D organizations. As chairman of DCRIPT company,Thierry will support EvidentIQ's BD activities and portfolio strategy as a consultant.


The Patient Insights Company

Carenity is a leading social platform supporting 500,000 patients and caregivers worldwide, across 1,200 chronic and rare diseases.

Founded in 2011 and headquartered in Paris, Carenity provides direct, timely and compliant access to patient real-world data.