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 

100% Configurable, Multi-Tenant eCOA is Here.

YPrime takes a significant leap into the future of clinical trial data capture with the most advanced, 100% configurable, multi-tenant eCOA platform. YPrime eCOA supports both complex and simple studies, delivering unparalleled benefits to patients, sites, and sponsors alike.

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Setting a New Standard in Clinical Trial Outcome Assessments.

96% say data
quality
is #1 factor

when choosing eCOA.2

76% say ease 

of use
is #2 factor

when choosing eCOA.2

72% say the ability to handle changes quickly 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 schedule, and obtain full oversight of trial progress.

Effortless Participant Management

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

Flexible Scheduling

Easily adapt visit schedules to support participants and enhance 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 schedule, and obtain full oversight of trial progress.

Effortless Participant Management

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

Flexible Scheduling

Easily adapt visit schedules to support participants and enhance 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.

The industry’s most advanced eCOA platform, enabling 100% configuration, was purpose-built for faster implementation and easy study changes. YPrime’s no-code, fully configurable nature allows for quick study launches, reducing startup times by 47%. 

Eliminate lack of flexibility of coding-based systems
Accelerate protocol amendment implementation
Minimize user acceptance testing (UAT) time

Improve Operational Efficiency
and User Experience.

A user-friendly eCOA is key to driving engagement and compliance—ensuring high-quality data. Our multi-tenant solution ensures all studies run on the same version, delivering consistency across portfolios. Our eCOA platform delivers:  

Consistent user experience with a unified portal and tablet interface—eliminating the need for extensive training
Intuitive interface that improves completion rates
Multilingual support with features that enable inclusivity and participation

Clinical Quality is at Our Core.

Quality is integral to clinical trial success. Our eCOA platform  
empowers you with the tools and transparency to ensure the  
highest clinical trial data quality for regulatory approval. From an advanced data warehouse and site performance monitoring functionality to compliance monitoring for risk mitigation, YPrime eCOA empowers clinical trial sponsors to:  

Proactively identify issues and take preventive measures to ensure data integrity
Benefit from combined learnings of our entire user base through a secure, multi-tenant approach
Experience the highest quality standards in the industry with top-tier benchmarks

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 Saster 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

Successful
eCOA Rescue.

A top pharma company needed a speedy eCOA rescue 
for a Phase 3 study with 216 sites and 900 patients, all across 
34 countries. 

We delivered:

Our pre-validated eCOA platform
Pre-configured for fast protocol amendments
With guidance from our therapeutic experts

With measurable results:

Reduced clinical trial timelines
Improved data quality
Maximized retention with a patient-centered experience
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 trial design, 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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