Solving for

Streamline your clinical trial technology.
Deliver 50% faster IRT and eCOA study startup.
Increase certainty from study design to data lock.

Certainty.

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YPrime continues to demonstrate its unique ability to improve patient participation and engagement in clinical trials, solidifying its position as a leader in clinical trial technology.

Patient Engagement

As Trailblazer In

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YPrime Recognized

Gain insights directly from clinical site personnel that can help you select technologies to boost trial efficiency as well as site and participant satisfaction.

to Informed Technology Investments

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A Sponsor's Guide

Solving for Certainty

AT YPRIME, WE

Increase
speed

to accelerate eCOA and IRT implementation.

Empower
flexibility

to support your clinical trials through protocol
amendment.

Inspire 
certainty

to empower you with better clinical trial outcomes.

YPrime’s eCOA, IRT, and eConsent enable faster study startup, high-quality data, and operational efficiencies.

Unmatched, 100% configurable, no-code eCOA platform reduces launch times by up to 47%.

Industry-leading IRT platform enables accelerated protocol amendment edits, improving study timelines.

Intuitive eConsent makes enrollment seamless, driving compliance and ease for patients and sites alike.

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Patient Engagement

faster

IRT startup times

swifter

protocol amendments

configurable

IRT and eCOA with pre-validated code

Clinical consulting—
expertise delivered.

Optimize clinical trial processes.

Customize data collection.

Seamlessly integrate systems.

Gain actionable insights to improve decision making.

Get Started

Clinical consulting
— expertise delivered.

Optimize clinical trial processes.

Customize data collection.

Seamlessly integrate systems.

Gain actionable insights to improve decision making.

Get Started

“One thing that I love about YPrime is that as a small site, when I need help and I need to contact Support, it’s quick, it’s easy, and it’s efficient.”

— Alexandria Clark, BSE, CCRC, Co-CEO, One of a Kind Clinical Research Center (1-OAK)

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

“We’ve used YPrime eCOA before and it has been the best eCOA experience we have ever had in a study.”

— Anna Fehr, RN, BSN, CCRC, Co-CEO, One of a Kind Clinical Research Center (1-OAK)

No other data science team at any other eCOA company helps construct data standards for my studies.
– Top 15 Pharma Customer

Certainty in clinical trial outcomes—
that’s what we do.

There’s no one-size-fits-all at YPrime—our technology and solutions allow us to customize an approach that works best for you.

740+

Studies
Implemented Globally

10+

Years IRT and
eCOA Experience

83

Countries

100k+

Patients Engaged

19

Therapeutic Areas

Certainty in clinical trial outcomes—
that’s what we do.

There’s no one-size-fits-all at YPrime—our technology and solutions allow us to customize an approach that works best for you.

740+

Studies
Implemented Globally

10+

Years IRT and
eCOA Experience

83

Countries

100k+

Patients Engaged

19

Therapeutic Areas

Let’s talk.

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!

Looking for ideas and inspiration
to improve your clinical trials?

Access our white papers, case studies, and blogs to discover new ways to solve for certainty in clinical trials.