eCOA health questionnaire on mobile phone screen

Fast, Flexible eCOA for Global Trials

Streamline Patient Data Capture. Deliver High-Quality eCOA.

Clinical trials are more complex—and more critical—than ever. YPrime’s electronic Clinical Outcome Assessment (eCOA) platform is purpose-built to help you move faster, capture better data, and meet patient needs globally. With advanced flexibility, scalability, and intuitive design, YPrime gives your team the tools to deliver confident results at every stage of the trial.

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The Future of Clinical Trial Data Capture 

eCOA Built for Speed, Flexibility, and Clinical Trial Certainty.

Launching a global study or making mid-study adjustments? YPrime’s fully configurable eCOA platform is built to adapt, accelerate, and deliver results.

Global-Ready: Translated and localized across 250+ languages
Built for Change: Quickly adapt to protocol amendments without disruptions
Pre-Validated Libraries: Accelerate startup with reduced translation and validation requirements
Patient-First: Intuitive navigation improves compliance and data integrity

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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 clinical trial progress.

Computer monitor displaying YPrime’s eCOA portal, showing participant workflow management, visit scheduling, and clinical trial progress tracking

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.

Near 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 clinical trial progress.

Computer monitor displaying YPrime’s eCOA portal, showing participant workflow management, visit scheduling, and clinical trial progress tracking

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.

Near 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 →

Configurable, Scalable eCOA That Adapts to Your Protocol.

Every study is different. YPrime’s flexible eCOA platform adapts to your protocol, region, and patient population—without slowing you down.

Seamless management of diverse device strategies
Support for complex, long-duration, and high-enrollment studies
Full scalability across therapeutic areas, geographies, and study phases
Deep experience in CNS, metabolic disease, oncology, and rare indications

A Patient-Centered Approach Drives Compliance and Data Quality.

A positive patient and site experience leads to stronger compliance and better data. YPrime’s patient app is developed with real-world usability research to support participants everywhere.

Clear Navigation: Step-by-step prompts and smart notifications guide participation
Device Agnostic: Support for BYOD or fully provisioned devices
Connected Devices: Integrations with wearables, glucometers, and more
Global Access: Multi-language localization for truly global trials

eCOA Reporting That Powers Decisions.

Turn raw clinical data into near real-time insights that drive smarter oversight, faster interventions, and better outcomes. Traditional eCOA platforms leave sponsors waiting for answers. Built with global inspection-readiness in mind, YPrime’s built-in reporting tools give you instant access to the information you need to act decisively throughout your trial.

Lightning-Fast Access: View data instantly—even across millions of entries
Customizable Dashboards: Filter, drill down, and visualize by site, subject, visit, or form
Compliance Monitoring: Spot trends, trigger alerts, and support early action
Audit-Ready Trails: Track every system interaction, update, and correction with full transparency

Want a preview? Book a demo of our eCOA reporting dashboards.

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    

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    

Future-Ready eCOA—Built for What’s Next in Clinical Trials.

47% faster study startup

100+ countries supported

BYOD and provisioned device ready

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.

Smiling young woman holding a smartphone, representing patient engagement and rapid eCOA deployment in a global Phase 3 clinical trial rescue

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

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

14+

Years eClinical Technology and Services

Future-Proof Your Trials with
Adaptive, Innovative eCOA Technology.

Clinical research is evolving. With YPrime, you’ll be set up for success with eCOA built to adapt to industry changes. Let’s get started!

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. 

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