Remove barriers for electronic consent management throughout clinical trial enrollment and participation. Meet participants wherever they are, on any device, with media-rich content to suit different learning styles. Nothing to download or install:
Include images, audio and video in eICFs
Verify comprehension with embedded questions
Automate eICF notifications and reminders
Support a multilingual experience
Overcome Informed Consent Challenges in Clinical Trials
Purpose-built solution to make informed consent easier, efficient and more engaging. eConsent is ready for:
Multiple trial settings – DCT, remote, in-person and hybrid
Global studies with multilingual populations
Single or multiple signature needs
Constant protocol changes and evolving informed consent requirements
Complete eConsent Platform for Streamlined Clinical Trials
Unified clinical workflows mean no more wasting time logging in and out of different systems. Seamless integration enables clinical trial study teams to easily see informed consent status in real-time. When protocols and requirements change, re-consenting workflows automatically trigger to help keep studies on track.
Data Privacy & Compliance
OpenClinica Consent delivers:
Data privacy and security in compliance with HIPAA and GDPR
Electronic signatures and audit logs in compliance with 21 CFR Part 11
Automated delivery of signed digital copy to participant
ISO 27001 and SOC2 security certification
Easy for participants and study teams.
Deliver on the true purpose of electronic informed consent in clinical trials.
Secure & Compliant
Compliant with HIPAA, GDPR, 21 CFR Part 11, ISO 27001, SOC 2.
Request a Free Trial
Experience and explore our powerful AND easy platform at your own pace