Medrio ePRO: Improve Your Patient Engagement

The Value of Patient-Reported Outcomes

As the value of patient-reported outcomes is becoming accepted as a critical component by which efficacy outcomes are measured, implementation changes still pose barriers during a clinical trial set up and data collection phases. Traditional methods increase the risk of missing patient safety signals and survey compliance considerations introduce additional complexity into trial design. Streamline the electronic collection of patient-reported data through Medrio’s unified ePRO and EDC platform that can be used anywhere and on any device.

Medrio ePRO

Our Electronic Patient-Reported Outcomes solution handles all of the complexities of patient-reported data, from the flexibility to switch between in-clinic and remote data collection, to the ability to support popular validated survey instruments. Our bring your own device (BYOD) model allows patients to respond to surveys anywhere at any time. Automated notifications ensure compliance with your protocol while boosting patient engagement. The unification of ePRO and EDC allows you to view all of your clinical and patient-reported data in one place and accelerates study build times. Gain faster insights into patient-reported data, more control over timelines, and increased patient engagement.

Trusted Experience

Medrio ePRO has supported 330+ studies across all therapeutic areas and stages of research.
Our experts have over 25 years of combined ePRO/eCOA experience to help navigate regulatory guidelines, study design, licensing, and more.
Support common validated survey instruments such as EQ5D, SF-12, and FACT scales

Improved Engagement

Collect data from anywhere- at home, work, or in-clinic on whichever device meets your patients’ needs
Improve adherence with flexible scheduling based on patients’ timezones, closeout windows that support time-sensitive data collection, and notifications that integrate with each patient’s lifestyle.

Unified System

Simplify set-up and eliminate the need for multiple vendors, UAT, and training coordination.
Improve patient safety and adverse event (AE) detection with real-time access to clinical and patient-reported data in one platform.
Less required vendor management gives you more time to focus on what matters: the patients.