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Solve for
Research.
Data Certainty.
Trial delays, protocol amendments, data quality—the challenges you face running clinical trials are daunting. With YPrime's technology platform, we empower you to streamline processes and solve for certainty.
YPrime Technology Platform
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 data2
41% say protocol amendments are the #3 concern
Multiple protocol amendments3
We empower you to solve for certainty, enabling 50% faster IRT startup times and up to 30% faster eCOA launch times than industry norms.
We empower you to solve for certainty, enabling 50% faster IRT startup times and up to 30% faster eCOA launch times than industry norms.
We accelerate start-up with eConsent
to make your enrollment seamless, without delays.
We accelerate start-up with eConsent
to make your enrollment seamless, without delays.
Then we reduce complexity in IRT…
to make your enrollment seamless, without delays.
When you’re ready for high-quality eCOA…
we enable 25% faster startup than industry norms
Along the way, we build engagement into everything
to help you consistently hit each clinical trial milestone.
Then, we reduce complexity in IRT…
to help you handle protocol amendments quickly.
Then, we reduce complexity in IRT…
to help you handle protocol amendments quickly.
When you’re ready for high-quality eCOA…
we enable 25% faster startup than industry norms.
Along the way, we build engagement into everything
to help you consistently hit each clinical trial milestone.
No other data science team at any other eCOA company helps construct data standards for my studies.
Top 15 Pharma CompanyCompany Name
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. Rest assured, your clinical trial data is always in compliance with ever-changing regulations.
650+
Studies Implemented Globally
19
Therapeutic Areas
10+
Years IRT and eCOA Experience
Let’s talk.
We’ve got you covered with strategies and solutions to improve your clinical trial operations, reduce site burden, and transform your patient experience. Let’s get started today!
