Speed, flexibility, and oversight are built into every part of your eCOA, IRT, eConsent, and participant-engagement workflows. In oncology, rare disease, CNS, cardiometabolic, vaccines, ophthalmology, and across complex global studies, YPrime gives sponsors and CROs the confidence to execute with certainty.
With configurable architecture, integrated data flows, and consistent global delivery, YPrime helps clinical trial teams move faster, from study startup through closeout—while eClinical technology that enables data quality at every step.
“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.
Experience That Matters.
~1,000
Studies Implemented Globally
15+
Years eClinical Technology and Services
100+
Countries
125K+
Patients Engaged
19+
Therapeutic Areas
Experience That Matters.
~1,000
Studies Implemented Globally
15+
Years eClinical Technology and Services
100+
Countries
125K+
Patients Engaged
19+
Therapeutic Areas
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!
