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.

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

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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

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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.

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