Easily manage all your clinical trials. Build, collect, monitor, share and manage data within one platform: user-friendly, secure, and compliant. Increase productivity and data quality with our unified eCRF, ePRO, eConsult, and eConsent solutions.
Speed up your clinical trials with our flexible and scalable EDC platform created for and by experts!
A new level of quality for your Clinical Trials
eCRF - EDC Platform
eCRF, a complete toolbox for clinical data collection
Quickly create your study forms with an infinite number of possibilities. Easily collect and monitor your studies and data in real time (Progress, Queries, Status, Automations, etc.).
eConsent
Secure Electronic Informed Consent
Take advantage of a secure and reliable eConsent solution for your informed consents. You are just a few clicks away from recruiting and starting your study!
ePRO - eCOA
New generation participant questionnaires and surveys
Discover a tailored, easy-to-use, user-centric survey solution (ePRO) to increase participant engagement and collect real-life data : feedback, evaluation, clinical experience…
eConsult
Teleconsultation and personalized participant follow-up
Access to high performance HD teleconsultation. Follow up with your participants in complete security and improve their engagement. Identity verification, support for signing electronic informed consent, real-time data collection…
What if you could manage your clinical trials more easily?
Adopt an effective clinical trial management solution now.
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