Multiple devices displaying YPrime’s clinical trial platform interface, including laptop, tablet, and mobile screens, highlighting seamless access and user-friendly design across platforms

Clinical Trial Technology Platform for Data Certainty.

Trial delays, protocol amendments, and data quality challenges put constant pressure on clinical trial teams. YPrime’s clinical trial technology platform helps sponsors and CROs move faster, with eCOA, IRT, and eConsent that deliver data integrity, inspection readiness, and execution confidence.

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Multiple devices displaying YPrime’s clinical trial platform interface, including laptop, tablet, and mobile screens, highlighting seamless access and user-friendly design across platforms
The top clinical trial technology challenges sponsors face…

62% say timeline/delays
are the #1 issue

Many clinical trials fall behind schedule1

50% say data-change capabilities are the
#2 problem

Limited flexibility puts data quality at risk1

41% say protocol amendments are the #3 concern

Frequent amendments disrupt trial execution1


A Clinical Trial Technology Platform—Built for Speed, Flexibility, and Certainty

At YPrime, we empower clinical trials
with eCOA, IRT, and eConsent, designed to reduce complexity across the study lifecycle while delivering reliable, inspection-ready data.

Accelerate startup
with eConsent

Streamline enrollment with intuitive electronic consent that improves participant understanding, speeds site workflows, and supports global compliance—so studies start faster and stay on track.

Electronic patient signature on tablet screen, representing eConsent for faster clinical trial enrollment and improved participant engagement

Accelerate startup
with eConsent

Streamline enrollment with intuitive electronic consent that improves participant understanding, speeds site workflows, and supports global compliance—so studies start faster and stay on track.

Reduce operational complexity with IRT

Manage randomization, supply workflows, and protocol changes with confidence. YPrime IRT is designed to support evolving study designs without disrupting timelines or data flow.

Empower high-quality data with eCOA

Launch faster with a purpose-built eCOA solution that supports complex protocols, global studies, and strong participant compliance—helping teams capture consistent, reliable data from first patient in through database lock.

With engagement built into every workflow

Across eConsent, IRT, and eCOA, YPrime embeds participant and site engagement into the platform—supporting adherence, reducing burden, and improving data completeness throughout the trial.

Illustration of a diverse patient population representing streamlined patient randomization and drug supply management in clinical trials

Reduce operational complexity with IRT

Manage randomization, supply workflows, and protocol changes with confidence. YPrime IRT is designed to support evolving study designs without disrupting timelines or data flow.

Reduce operational complexity with IRT

Manage randomization, supply workflows, and protocol changes with confidence. YPrime IRT is designed to support evolving study designs without disrupting timelines or data flow.

Empower high-quality data with eCOA

Launch faster with a purpose-built eCOA solution that supports complex protocols, global studies, and strong participant compliance—helping teams capture consistent, reliable data from first patient in through database lock.

Mobile phone displaying an eCOA questionnaire screen, representing faster clinical trial startup and streamlined data collection
Engagement module graphic illustrating participant and site involvement in clinical trials to support milestone achievement and data quality

With engagement built into every workflow

Across eConsent, IRT, and eCOA, YPrime embeds participant and site engagement into the platform—supporting adherence, reducing burden, and improving data completeness throughout the trial.

All this in an industry-leading
clinical trial technology platform

With unified data flows and real-time visibility, YPrime helps clinical trial teams act with confidence—turning operational complexity into clarity across every phase of the study.

Unified diamond graphic representing YPrime’s integrated clinical trial platform with eConsent, IRT, eCOA, and patient engagement solutions for data certainty and actionable insights

All this in an industry-leading
clinical trial technology platform

With unified data flows and real-time visibility, YPrime helps clinical trial teams act with confidence—turning operational complexity into clarity across every phase of the study.

Unified diamond graphic representing YPrime’s integrated clinical trial platform with eConsent, IRT, eCOA, and patient engagement solutions for data certainty and actionable insights
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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 Group

Clinical Trial Technology Experience That Matters.

Globe icon representing the number of clinical studies implemented globally with YPrime’s technology platform

~1,000

Studies Implemented
Globally

Search icon representing the number of therapeutic areas supported by YPrime’s clinical trial solutions

19+

Therapeutic
Areas

Three stars with arrows icon representing YPrime’s years of experience in eClinical technology and services

16+

Years eClinical Technology
and Services

YPrime’s eCOA Portal 

—The New Standard

YPrime redefines clinical trial efficiency with an eCOA portal that empowers sponsors and sites to quickly and seamlessly manage participant workflows, maintain visit schedule, and obtain full oversight of trial progress.

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We help pharma companies, emerging biotechs, and CROs simplify clinical trial technology, reduce site burden, and improve participant experience—without compromising data quality or compliance.

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Explore Insights from Our Experts.

Gain valuable perspectives on clinical trial design, high-quality data capture, operational efficiencies, and, ultimately, how to solve with certainty in clinical research.

Source:

1 YPrime Clinical Trial Survey, 2023.

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