eCOA / ePRO
Empower participants, clinicians, and observers. Enable convenient and accurate outcome reporting, enhancing data quality and study efficiency with electronic patient reported outcomes (ePRO) and electronic clinical outcome assessments (eCOA).
Increase Participant Engagement
Participation is made easy with a web-based, device-agnostic solution.
Support Complex Protocols
Collect data in-clinic or remotely with validated and home-grown surveys.
Access Clinical Data in Real Time
View data to make real-time decisions with zero delays between collection and monitoring.
Improve Outcomes
Flexible Features for Faster Clinical Trials
An intuitive, configurable solution built to improve the participant experience, site processes, and data quality from protocol to postmarket.
- Build and reuse assessment templates with no custom coding required
- Engage participants on any web-enabled device
- .Seamlessly integrate wearable and outside data with the back-end database
Stronger Clinical Evidence with Electronic Patient Reported Outcomes
Demonstrate value to regulators and payors with high-quality data from eCOA / ePRO clinical trials. An easy-to-use interface, automated notifications, and the MyMedrio participant portal improve participant compliance and retention.
Accelerate Study Startup
Set up in as little as four weeks, accelerating the time it takes to begin capturing data. Quick, intuitive survey builds ensure you meet study timelines, ultimately reducing costs. Meanwhile, robust support helps you adhere to study protocols and industry standards.
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