Clinical Trial Consulting– Expertise Delivered.

You’re almost there. You’ve developed your molecule, and now it’s time to kick off your clinical trial journey. But, where do you begin? Are you certain of your clinical trial design? Are your processes built to drive data quality and informed decisions?

Get Started

Focus on science.
We’ll handle the processes.

At YPrime, we streamline your clinical trial journey, increasing certainty from study design to data lock. With nearly two decades at the forefront of clinical trials, we look ahead and design research studies to minimize challenges and solve for certainty.

Focus on science.
We’ll handle the processes.

At YPrime, we streamline your clinical trial journey, increasing certainty from study design to data lock. With nearly two decades at the forefront of clinical trials, we look ahead and design research studies to minimize challenges and solve for certainty.

Your data challenges solved.

Data standardization

Globally, regulatory agencies require standardized submissions—and the requirements are expanding. We implement data standards to meet trial needs, ensuring your trial is submission-ready.

Data management

Data is your most powerful asset. We are here to help you make informed decisions through system integration support, program design, process optimization, and tailored governance strategies.

Data monitoring

Every clinical trial needs a warning system to catch risks. Our data monitoring team empowers you to see the unseen, anticipate the unexpected, and navigate your trial with certainty.

Statistical support

We support you with a full suite of expert services—from population design and sample size calculation, to randomization and reporting. Whether you need a simple randomization list or complex simulations, we’ve got you covered.

We’re the team to
help you solve.

We save
you time

by leading your system implementations.

We help
you drive strategy

with our deep therapeutic expertise.

We enable data-driven decisions

helping you solve for clinical trial certainty.

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. From trial design to data lock, our consulting experts are available every step of the way.

740+

Studies Implemented Globally

19

Therapeutic
Areas

10+

Years IRT and
eCOA Experience

Let’s solve for 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. Our unified eConsent, IRT, and eCOA platform helps you deliver the clinical trial outcomes you need. Let’s get started!

Check out what our experts have to say

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

Clinical Trial Consulting– Expertise Delivered.

Focus on science.
We’ll handle the processes.

At YPrime, we streamline your clinical trial journey, increasing certainty from study design to data lock. With nearly two decades at the forefront of clinical trials, we look ahead and design research studies to minimize challenges and solve for certainty.

Focus on science.
We’ll handle the processes.

At YPrime, we streamline your clinical trial journey, increasing certainty from study design to data lock. With nearly two decades at the forefront of clinical trials, we look ahead and design research studies to minimize challenges and solve for certainty.