Introducing TrialConsent TM 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 .

Minimize Regulatory Risk
Mitigate risk of fines, delays and litigation. Digital timestamps, version control and real-time remote monitoring all work to provide a clean audit trail.
Enhance Understanding
Improve recruitment and retention rates by providing prospective participants clear and easy-to-understand information so that they can make an informed decision.
Reduce Costs
Minimize the need for on-site consent monitoring, improve retention rates and mitigate the risk of regulatory and litigation-related expenses. TrialConsent™ limits costs while protecting the integrity of your clinical trial from the start.
Streamline Development
Align and expedite the consent development, approval, deployment and documentation process with the TrialConsent™ design tool. Collaborate easily across sponsors, sites and ethics committees to ensure participants receive standardized, up-to-date and accurate information.
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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