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


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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.

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.

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 .

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
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*We respect your privacy and will never share any information you provide us. Privacy Policy

CRF Health is a leading provider of electronic Clinical Outcome Assessment (eCOA)  and electronic informed consent solutions for global clinical trials. With experience in more than 800 trials, over 100  languages and across 74 countries, CRF Health’s TrialMax® platform consistently demonstrates the industry’s highest data accuracy, patient and site compliance, and patient retention.


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