eConsent is gradually emerging as an essential evolution of informed consent in clinical research.
But what does the regulation actually say? What tangible benefits can be achieved? And how can it be implemented smoothly, without disrupting your current processes?
In this Datacapt webinar, our experts will help you demystify the topic:
- Understand the real legal framework in France, Europe, and the United States.
- Identify concrete benefits for patients, sites, and sponsors.
- Discover how study teams are adopting eConsent easily, without technical complexity.
A clear, educational, and inspiring session designed for CROs, Sponsors, and Clinical Research Teams who want to combine innovation, compliance, and patient experience.
Register now and transform your vision of informed consent
👉 GET MY FREE SEAT
Please note that it will be a French speaking event
