Book a tailored walkthrough and we'll show econsent configured around your protocol.
eConsent removes the biggest source of protocol deviations at most sites: Incomplete or outdated paper consent. The PI and CRC author each ICF version once on the desktop console, attach explainer media, and publish it to the right cohorts. Subjects then complete consent on their own device, on-site on a tablet or remotely from home, while the platform enforces that the current approved version is always the one being signed. When the protocol changes, re-consent is pushed automatically and every subject’s status is tracked until closed.
eConsent
Purpose-built for hybrid & decentralized trials. One workflow across desktop and mobile.
eConsent works across the ProCTTH hybrid platform. Site staff (CRC, PI, CRA) work on the desktop web console, while subjects access the study from the mobile app.
CRC · PI · CRA
Subject
Subjects open the study app, read the consent at their own pace in their language, complete comprehension checks, and sign with a compliant e-signature; on-site or from home.
PI/CRC create the ICF, add explainer videos and FAQs, and lock the approved version on the web console
The correct consent version is pushed to each subject's mobile app, in their preferred language.
Subjects read, complete comprehension checks, and apply a compliant e-signature from any device.
Sites monitor completion and the platform auto-pushes re-consent whenever the protocol changes.
Streamlined subject enrolment from screening to randomisation, all from a single guided workflow.
