An eCOA platform designed with you in mind.
97% say data
quality
is #1 factor
when choosing eCOA2.
90% say ease
of use
is #2 factor
when choosing eCOA2.
88% say faster
start-up
is #3 factor
when choosing eCOA2.
Configurability Delivers Flexibility, Speed and Speed.
YPrime’s eCOA platform was purpose-built for faster implementation and to easily make study changes.
User Experience
Drives Compliance.
At YPrime, we know that a user-friendly eCOA platform is key to driving participant engagement and compliance—ensuring high-quality data. Our solutions prioritize:
Quality is at Our Core.
Quality is integral to clinical trial success. At YPrime, we empower you with the tools and transparency to ensure the highest data quality for regulatory approval:
Accelerate your trial timelines.
Improve your data capture.
Drive
Up to 30% faster
startup times
with our pre-validated eCOA libraries.
Ensure
high-quality
data
with built-in validation.
Simplify
user
experience
with our easy-to-use interface.
It’s YPrime that solves for certainty in clinical trial outcomes.
There’s no one-size-fits-all at YPrime—our technology and solutions allow us to customize an approach that works best for you, helping you enhance patient engagement and improve visit compliance.
650+
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 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.
Sources
- https://ncbi.nlm.nih.gov/pmc/articles/PMC9293739/
- YPrime Clinical Trial Survey, 2023