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?
Your Clinical Trial Data Challenges Solved.
Clinical data standardization
Globally, regulatory agencies require standardized submissions—and the requirements are expanding. We implement clinical data standards to meet trial needs, ensuring your trial is submission-ready.
Clinical data management
Clinical 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.
Clinical data monitoring
Every clinical trial needs a warning system to catch risks. Our clinical 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
That help 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 clinical trial 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.
