Introducing TrialConsent® from CRF Health, a Revolutionary eConsent Solution.
Because informed consent takes more than a signature.

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TrialConsent from CRF Health simplifies informed consent for sponsors, site teams and ethics committees with an easy-to-use, powerful platform.

Intuitive and interactive, TrialConsent promotes participant compliance and retention through better comprehension. It's the only electronic informed consent solution that can serve as a standalone solution or fully integrate with eCOA .

Flexible Signature Solutions
Obtain the benefits of document management and control, electronic storage, and centralized monitoring even for paper consent forms. Ensure full global acceptance through three approaches to consent form signature: Digitized electronic signatures, Print-to-sign, Offline Paper Consent
Collaborative Streamlined Approval Process
Collaborate digitally on the development and approval of your informed consent documentation with sites and IRBs/ECs.
Available as Self-Service or Full-Service
Use your existing infrastructure to develop your own consent forms and documentation, create libraries for easy re-use across studies and maintain full control over your processes through our self-service platform. Alternatively, let our experienced operational team manage the entire development and implementation process for you.
Reduce Consent Document Management Complexity
Manage consent document versions for multiple countries and sites, and seamlessly manage consent form updates and re-consenting efficiently within a single system.
eCOA and eConsent on One Device
Reduce cost and lower burden for site staff by leveraging a single provisioned device for electronic informed consent and site-based electronic clinical outcome assessments (eCOA) using CRF Health’s single platform.
Save time by expediting consent development, approval, deployment and documentation with the proprietary TrialConsent design tool.
The collaborative design process and user-friendly interface make it easy for sponsors, sites, and IRBs/IECs to work together efficiently.
Real-Time Consent Monitoring
Comprehensive reporting enables study teams and ethics committees to monitor the consent status of sites and participants, track and analyze compliance and make smarter decisions.

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