eCOA health questionnaire on mobile phone screen

YPrime eCOA Enables 30% 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, 100% configurable eCOA platform—built to enable faster study startup, high-quality data, and operational efficiencies.

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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—enabling faster study startup, high-quality data, and operational efficiencies.

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A New Standard in Clinical Trial Outcome Assessments.

97% say data
quality
is #1 factor

when choosing eCOA2.

90% say ease 

of use
is #2 factor

when choosing eCOA2.

88% say faster
startup
is #3 factor

when choosing eCOA2.

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 up to 30%. 

Eliminate lack of flexibility of coding-based systems
Accelerate protocol amendment implementation
Spend less time on UAT

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 that 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 interfaces that improve completion rates
With multilingual support and features that ensure inclusivity and participation

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 data quality for regulatory approval. From an advanced data warehouse and site performance monitoring functionality to compliance monitoring for risk mitigation, YPrime’s eCOA platform 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 quality benchmarks

Pre-Validated, Configurable eCOAs For Faster Startup.

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

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Accelerate Your Trial Timelines.
Improve Your Data Capture.

Drive
Up to 30% faster
startup times

with our 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 Your Data Capture.

Drive
30% faster

startup times

with our pre-validated eCOA libraries.

Ensure
high-quality
data

with built-in validation.

Simplify
user
experience

with our easy-to-use interface.

CASE STUDY

How we solved
for certainty—
an eCOA rescue.

A top pharma company needed a speedy eCOA rescue
for a Phase 3 study, with 216 sites, 900 patients, 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:

Reduce clinical trial timelines.
Improve data quality.
Maximize 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 CustomerCompany Name

It’s YPrime that solves for certainty in clinical trial outcomes.

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

650+

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 in compliance and that the process will be easy. Our eConsent, IRT, and eCOA platform helps you deliver the clinical trial outcomes you need. Let’s get started!

Check Out What Our Experts Have to Say

about trial design, data capture, operational efficiencies, and, ultimately, solving for certainty in clinical research.

Sources

  1. https://ncbi.nlm.nih.gov/pmc/articles/PMC9293739/
  2. YPrime Clinical Trial Survey, 2023
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