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Clinical Trial Technology That Solves for Data Certainty.

Trial delays, protocol amendments, data quality—the challenges you face running clinical trials are daunting. With YPrime’s clinical trial technology platform, we empower you with eCOA, IRT, and eConsent to streamline processes and solve for certainty. 

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Top 3 issues keeping 

clinical leaders up at night…

62% say timeline/delays
are the #1 issue

Most studies are behind schedule1

50% say data-change capabilities are the
#2 problem

They need high-fidelity data1

41% say protocol amendments are the #3 concern

Multiple protocol amendments impact timelines1

At YPrime, we empower you with
eCOA, IRT, and eConsent, with built-in engagement to drive speed, flexibility, and certainty in clinical research. 

First, we accelerate startup
with eConsent…

to make your enrollment seamless and timely, enhancing participant engagement while maintaining compliance. 

First, we accelerate startup with eConsent…

to make your enrollment seamless and timely, enhancing participant engagement while maintaining compliance. 

Then we reduce complexity in IRT…

to streamline patient randomization and drug supply management with a solution that handles protocol amendments quickly—helping your trial stay on track. 

When you’re ready for high-quality eCOA…

we enable 47% faster startup than industry norms with a 100% configurable solution that empowers clinical trial teams to streamline data collection and improve user engagement.

Along the way, we
build engagement
into everything…

to help you consistently hit each clinical trial milestone, creating an environment that supports participant and site involvement and drives data quality. 

Then, we reduce
complexity in IRT…

to streamline patient randomization and drug supply management with a solution that handles protocol amendments quickly—helping your trial stay on track. 

Then, we reduce
complexity in IRT…

to help you streamline patient randomization and drug supply management, with a solution that handles protocol amendments quickly— helping your trial stay on track. 

When you’re ready for
high-quality eCOA…

we enable 47% faster startup than industry norms with a 100% configurable solution that empowers clinical trial teams to streamline data collection and improve user engagement.

Along the way, we
build engagement
into everything…

to help you consistently hit each clinical trial milestone, creating an environment that supports participant and site involvement and drives data quality. 

All this in one
technology platform…

we solve data certainty for you, delivering actionable insights and reliable results throughout your clinical trials. 

All this in one
technology platform…

we solve data certainty for you, delivering actionable insights and reliable results throughout your clinical trials. 

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YPrime’s clinical trial technology platform offers patient engagement features across eConsent and eCOA, leveraging user-friendly design, personalization, and behavioral science to drive patient retention and adherence.
Nisarg Shah, Practice Director, Everest Group

Certainty in Clinical Trial Outcomes—
That’s What We Do.

There’s no one-size-fits-all at YPrime. Our clinical trial technology and solutions allow us to customize an approach that works best for you. Rest assured, your clinical trial data is always in compliance with ever-changing regulations.

740+

Studies Implemented Globally

19

Therapeutic Areas

10+

Years’ IRT and eCOA Experience

Let’s talk.

We’ve got you covered with strategies and solutions to improve your clinical trial operations, reduce site burden, and transform your patient experience.
Let’s get started today!

Check Out What Our Experts Have to Say

about trial design, data capture, operational efficiencies, and, ultimately, solving for certainty in clinical research.

Source:

1 YPrime Clinical Trial Survey, 2023.

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