eCOA Platform | YPrime

Experience Next-Level Data

Certainty with

YPrime's

eCOA Platform.

$1-2 billion per new drug!¹ The cost for you to bring new medicines to market is unsustainable. That’s why our proven eCOA platform is built to give you certainty in data capture.

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Experience Next-Level Data Certainty with eCOA Platform.

An eCOA platform designed with you in mind.

97% say data
quality
is #1 factor

when choosing eCOA².

90% say ease  
of use
is #2 factor

when choosing eCOA².

88% say faster
start-up
is #3 factor

when choosing eCOA².

Configurability Delivers Flexibility, Speed and Speed.

YPrime’s eCOA platform was purpose-built for faster implementation and to easily make study changes.

Eliminate frustration and lack of flexibility of coding-based systems

Accelerate protocol amendment implementation

Spend less time on UAT

User Experience
Drives Compliance.

At YPrime, we know that a user-friendly eCOA platform is key to driving participant engagement and compliance—ensuring high-quality data. Our solutions prioritize:

A positive user experience, improving compliance

Reduced burden, with intuitive interfaces that improve completion
rates

And accessibility for all, with multilingual support and features that
ensure inclusivity and participation

Quality is at Our Core.

Quality is integral to clinical trial success. At YPrime, we empower you with the tools and transparency to ensure the highest data quality for regulatory approval:

Proactively identify issues and take preventative 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 start-up.

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

Get Started

Pre-validated, configurable eCOAs for faster start-up.

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

Get Started

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.

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.

400+

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!