Discover How YPrime Can Help You with Speed, Flexibility, and Certainty in Clinical Research.

At YPrime, we’re committed to helping you solve with certainty in clinical research. We are driven by the dedication of researchers seeking evidence, the needs of patients awaiting solutions, and the innovations brought by companies introducing groundbreaking products. Together, we can achieve greater certainty—delivering industry-leading eCOA, IRT, and eConsent.

Tech Support

Why Choose YPrime for Your Clinical Trials?

Increase Speed, Improve Quality, and Drive Certainty – With a Seamless User Experience Across eCOA, IRT, and eConsent:

Accelerate Trial Startup: Achieve 47% faster electronic Clinical Outcome Assessment (eCOA) startup times, streamlining your trial while enhancing efficiency.

Unmatched Flexibility and Data Quality: Our no-code, fully configurable Interactive Response Technology (IRT) and eCOA platform simplifies trial complexities, driving superior data quality. Experience unparalleled flexibility tailored to your trial’s needs, with pre-validated code built to maintain data accuracy.

Enhanced Patient and Site Engagement: Our patient-facing app and platform are designed to maximize patient and site participation, ensuring a smooth and engaging trial experience while improving compliance.

High Quality Data: Our people, processes, and technology drive the highest standards of quality and regulatory compliance.

Contact us today and let’s review your pipeline. We are here to help you improve your eCOA, IRT, and eConsent, with speed, flexibility, and certainty.

YPrime’s corporate headquarter is located at:
101 Lindenwood Drive, Suite 101,
Malvern, PA 19355