The ultimate guide to understanding and implementing eConsent.

Written by
Florentin Ory
Published on
July 22, 2025

Informed consent is a key step in clinical trials.
Its traditional paper format has limitations: lack of clarity, errors, administrative burden…What if you switched to digital?

With eConsent, streamline consent management while enhancing participant understanding and experience.

Let's Shape the Future of Clinical Trial Together!

A must-have guide for Sponsors, CROs, and Clinical Research professionals!

What you’ll discover in this practical guide:

  • The tangible benefits of eConsent
  • Key insights for international compliance (FDA, EMA, GDPR…)
  • Best practices for a successful and secure implementation
  • Essential criteria for choosing the right eConsent solution
  • Real-world feedback and case studies on eConsent adoption

Florentin Ory
CEO & Co-Founder

Florentin combines clinical research know-how with a true passion for product design. Attentive to detail and obsessed with user experience, he ensures that Datacapt remains a high-performance platform that’s also intuitive and accessible to every user.