[Webinar] Inclusivity in Clinical Research

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Inclusivity in clinical research is now a key factor in the quality of scientific results, the generalizability of those results, and the provision of better patient care. It aims to ensure that clinical trial participants accurately reflect the diversity of the general population and of patients affected by a disease.

F-CRIN invites you to explore the various dimensions of inclusivity in clinical research through three complementary themes during its upcoming webinar: 

  • Inequalities in inclusion in clinical trials: Current Situation & Opportunities for Action
  • Review of the F-CRIN networks’ commitment and feedback from the MUST network
  • Promoting Inclusivity: Regulatory Leverage

This new “F-CRIN Clinical Research Meeting” will provide you with key insights on how to collect sensitive data, include people in vulnerable situations, and better account for associated biases when interpreting results. This will be an opportunity to share initiatives and ideas for action aimed at making clinical research more accessible and relevant.

Do you have a question you’d like to ask in advance? Feel free to send it to us at contact.fcrin@inserm.fr

Interested? Join us on November 26, from 1:00 p.m. to 2:30 p.m.

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Updated on 22 October 2026