eConsent - end-to-end solution for consent process
eConsent is an innovative, regulatory-compliant, patient-friendly, electronic consent system for clinical trials
Build a streamlined and compliant consent process
Build a multi-page consent walkthrough tailored to the specifics of the study and participants. Provide accurate and tailored consents form based on site, rules, or patient demographics.
Notify participants for re-consent
Engage with participants by letting them know they have a new consent to consider. Make sure participants always get the last version.
Improve document management and control
IRBs, sites, and sponsors collaborate in a single system—review real-time consent drafting progress and performance metrics.
See Zapclinica
in action
A tour of Zapclinica just for you - how it works, and how it can meet your needs.
Part of the Zapclinica platform
Zapclinica helps you managing your clinical trial, reduces the time to market, the cost, and the burden to run a successful clinical trial by operationally streamlining every task in an all-in-one platform.
