Guide
The ultimate guide to understanding and implementing eConsent.
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.
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
