eCOA health questionnaire on mobile phone screen

Electronic Clinical Outcome Assessment

YPrime eCOA Enables 47% Faster Study Startup.

$1-2 billion per new drug!1 The cost for you to bring new medicines to market is unsustainable. That’s why at YPrime, we’ve delivered the most advanced, fully configurable electronic clinical outcome assessment (eCOA) platform—built to enable faster study startup, high-quality data, and operational efficiencies.

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The Future of Clinical Trial Data Capture 

Your Partner in Simplifying Clinical Trials With Speed, Flexibility, and High-Quality eCOA

Choosing the right eCOA provider is essential for clinical trial success. At YPrime, our eCOA platform delivers a proven solution designed to streamline complex trial processes, enhance data quality, and accelerate timelines. With patient-first design and global support, YPrime empowers your trials to run efficiently and deliver reliable outcomes.

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Setting a New Standard in Clinical Trial Outcome Assessments.

97% say data
quality
is #1 factor

When choosing eCOA.2

90% say ease
of use
is #2 factor

When choosing eCOA.2

88% say faster
study startup
is #3 factor

When choosing eCOA.2

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 schedules, and obtain full oversight of trial progress.

Effortless management

Intuitive tools enable quick setup and streamlined participant tracking, optimizing the site user experience.

Flexible scheduling

Easily adapt visit schedules to support site staff and participants—improving trial efficiency.

Real-time
insights

Access comprehensive trial data and dynamic reporting capabilities that enable informed decision-making and optimize trial outcomes through data-driven insights.

Schedule a Demo →

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 schedules, and obtain full oversight of trial progress.

Effortless management

Intuitive tools enable quick setup and streamlined participant tracking, optimizing the site user experience.

Flexible scheduling

Easily adapt visit schedules to support site staff and participants—improving trial efficiency.

Real-time
insights

Access comprehensive trial data and dynamic reporting capabilities that enable informed decision-making and optimize trial outcomes through data-driven insights.

Schedule a Demo →

Deliver Faster Study Startup.

YPrime delivers the industry’s most advanced eCOA platform, purpose-built to streamline study startup and simplify mid-study changes. Our fully configurable solution enables rapid implementation, reducing startup timelines by 47%. YPrime eliminates common barriers to trial readiness and ensures your study progresses without delays.

Break free from coding-based systems with a platform designed for seamless adaptability
Quickly implement mid-study changes without disrupting timelines, ensuring trials stay on track
Minimize user acceptance testing with pre-validated components, delivering faster go-live readiness

Improve User Experience.

A user-friendly eCOA is key to driving patient engagement. With a user-friendly design, our patient-centered app drives compliance, improves data quality, and supports diverse populations. Backed by extensive UX research, our platform delivers:  

An intuitive experience, supporting patients across all technical skill levels, with clear navigation, notifications, and step-by-step instructions
Connected device integrations to seamlessly enhance data collection, minimize patient burden, and unlock new possibilities for trial innovation
Global access, with multi-language support and localization for diverse patient populations, improving compliance

Meet Your Trial Needs With Flexibility and Global Scalability.

Every clinical trial is unique. At YPrime, our eCOA platform is built to adapt to meet your needs. Our flexible technology supports provisioned and bring-your-own-device (BYOD) strategies, ensuring accessibility for patients worldwide. With seamless multi-language localization, configurable workflows, and robust support across 195+ countries, we support trials globally.

Meet diverse patient needs with a seamless mix of device strategies
Multi-language capabilities and local support ensure smooth operations across regions
Our configurable platform aligns with evolving protocols and global regulations

Pre-Validated, Configurable eCOAs for Faster Startup.

Watch our video and discover how YPrime’s eCOA platform helps you solve for certainty, while reducing site and patient burden.

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Pre-Validated, Configurable eCOAs for Faster Startup.

Watch our video and discover how YPrime’s eCOA platform helps you solve for certainty, while reducing site and patient burden.

Get Started    

Accelerate Your Trial Timelines.
Improve Data Capture.

Drive
47% faster
startup times

With pre-validated eCOA libraries.

Ensure
high-quality
data

With built-in validation.

Simplify
user
experience

With our easy-to-use interface.

Accelerate Your Trial Timelines.
Improve Data Capture.

Drive
47% faster

startup times

With pre-validated eCOA libraries.

Ensure
high-quality
data

With built-in validation.

Simplify
user
experience

With our easy-to-use interface.

CASE STUDY

Rapid eCOA Rescue for a
Global Phase 3 Trial.

When a leading pharmaceutical company faced critical delays in a Phase 3 study spanning 216 sites and 900 patients across 34 countries, they turned to YPrime for a fast and effective eCOA solution. They needed a reliable eCOA platform to rescue the study, address protocol amendments, and ensure patient engagement and data quality.

We delivered:

Our pre-validated eCOA platform ready for immediate deployment
Pre-configured to handle complex study changes with ease
Strategic guidance from our therapeutic area specialists ensured seamless implementation

With measurable results:

Achieved rapid deployment and reduced trial delays
Delivered consistent, high-quality data for reliable insights and regulatory approval
Engaged patients with a user-friendly, patient-centered experience, maximizing study completion rates
YPrime has a clean and seamless UI. It is able to take the data and put it into graphs and figures to show where the data is trending.
– Head of Real-World Data Analytics, Top 20 Pharma Customer

It’s YPrime That Solves for Certainty in Clinical Trial Outcomes.

There’s no one-size-fits-all at YPrime. Our clinical trial technology and solutions allow us to customize an approach that works best for you, helping you enhance patient engagement and improve visit compliance.

740+

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 compliant. Our eCOA, IRT, and eConsent platform helps you deliver the
clinical trial outcomes you need. Let’s get started! 

Explore Insights From Our Experts.

Gain valuable perspectives on clinical trial design, high-quality data capture, operational efficiencies, and, ultimately,
solving for certainty in clinical research. 

Sources

  1. Why 90% of clinical drug development fails and how to improve it, 2022
  2. YPrime Clinical Trial Survey, 2023

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