electronic participant signature

Electronic Consent

Start Strong with an eConsent Platform that Drives Enrollment.

40% of all trial spend is on recruitment, with more than two-thirds of sites failing to meet enrollment goals.1 To streamline enrollment and improve costs, your electronic consent must be seamless. 

Get Started    

Make Enrollment Seamless with eConsent.

At YPrime, our eConsent solution streamlines informed consent in global clinical trials, enabling compliance and driving ease of use for patients and sites alike. Discover how YPrime delivers an intuitive, cost-effective electronic consent process that enhances the user experience while enabling regulatory compliance at every step. 

Get Started    

Make Enrollment Seamless with eConsent.

At YPrime, our eConsent solution streamlines informed consent in global clinical trials, enabling compliance and driving ease of use for patients and sites alike. Discover how YPrime delivers an intuitive, cost-effective electronic consent process that enhances the user experience while enabling regulatory compliance at every step. 

Get Started    
Simplify Your Clinical Trial Enrollment with Our
eConsent Platform. 
Computer screen icon displaying pie chart and bar graphs, representing dynamic clinical trial information for clear data visualization and communication

Present
dynamic
information

That clearly explains your trial.

Icons of computer, tablet, and mobile phone representing patient support across all devices, in any language and at their own pace

Support your
patients on
any device

In their own language and at their own pace.

Headset and chat bubble icon representing built-in patient support for clinical trials, available whenever assistance is needed

Deliver
immediate,
built-in support

When your patients need it most.

Let Our Clinical Technology
Platform Simplify
Your Trial Experience.

Deliver the same user experience across eConsent, eCOA, and IRT modules
Guide your patients through a seamless journey to reach each trial milestone
Quickly access reports from consent and randomization to outcome capture
Female patient electronically signing a consent document on a smartphone, representing streamlined eConsent in clinical trial technology
Clinician using a tablet to manage electronic consent, ensuring clinical trial data integrity and regulatory compliance

Enhance Clinical Trial Integrity with YPrime’s eConsent Solution.

Navigating regulatory requirements is daunting. At YPrime, we ensure electronic consent is obtained legally and ethically, regardless of location, providing certainty in the integrity of your clinical trial data.

At YPrime, data security is at our core. All data in our platform is encrypted, and every version change is stored for future compliance needs or audits.
– David Wallace, Chief Technology Officer, YPrime

Let’s Solve with Certainty in Clinical Research—Together!

When we work together, you know that your clinical trial data is always in compliance and that the process will be easy. Let’s get started!

Explore Insights from Our Experts.

Gain valuable perspectives on clinical trial design, high-quality data capture, operational efficiencies, and, ultimately, how to solve with certainty in clinical research.

Sources:

1Considerations For Improving Patient Recruitment Into Clinical Trials

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