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Clinical Trial Technology that Solves with 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 with 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

Experience That Matters.

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~1,000

Studies Implemented
Globally

19+

Therapeutic
Areas

14+

Years eClinical Technology
and Services

YPrime’s eCOA Portal 

—The New Standard

YPrime redefines clinical trial efficiency with an eCOA portal that empowers sponsors and sites to quickly and seamlessly manage participant workflows, maintain visit schedule, and obtain full oversight of trial progress.

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

Let’s Talk

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.

Source:

1 YPrime Clinical Trial Survey, 2023.

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