eCOA / ePRO

The eCOA / ePRO software is designed to empower participants, clinicians, and observers by providing a convenient and accurate method for reporting outcomes. This enhances the quality of data and improves study efficiency using electronic patient-reported outcomes (ePRO) and electronic clinical outcome assessments (eCOA).

Increase Participant Engagement

The solution is web-based and device-agnostic, simplifying participation for users.

Support Complex Protocols

It allows for data collection both in-clinic and remotely, with options for validated or custom-made surveys.

Access Clinical Data in Real Time

Real-time data access facilitates immediate decision-making without delays in data monitoring.

Flexible Features for Faster Clinical Trials

This intuitive and configurable software enhances participant experiences, site processes, and data quality, from protocol development to postmarket stages. It allows the building and reuse of assessment templates without custom coding and supports participant engagement on any web-enabled device. Furthermore, it integrates seamlessly with wearable devices and external data sources into the back-end database.

Stronger Clinical Evidence

By utilizing eCOA / ePRO in clinical trials, stronger clinical evidence can be presented to regulators and payors. The software’s easy-to-use interface, automated notifications, and the MyMedrio participant portal all contribute to better compliance and participant retention.

Accelerate Study Startup

Studies can be initiated in as little as four weeks, expediting the data capture process and reducing costs. Quick and intuitive survey building meets study timelines, and robust support ensures adherence to study protocols and industry standards.

What Users Are Saying

Testimonials highlight ease of implementation, reliable support, and simplified data management. With a 98% customer retention rate, Medrio is noted for providing a consistent and supportive team throughout the study process.

Overall, the software is part of an integrated suite of solutions designed to maximize trial efficiency and excellence in clinical data management. It supports enhancing compliance through efficient informed consent management and optimizes study supply management to eliminate bias.