uMotif | eCOA/ePRO Platform

Delivering >90% compliance in real-world studies

Book a demo today and see how uMotif’s eCOA/ePRO platform drives unparalleled levels of patient engagement to transform the speed, quality and accuracy of data.

Who we are Read our case studies

Our eCOA/ePRO platform powers unrivaled patient engagement and is trusted by leading pharma & biotech organizations across the globe.

We are experts in real-world patient data capture, covering all aspects of RWE – observational research, long-term follow-ups, natural history studies, non-interventional trials, and registries. Our deep understanding and unique approach is proven to achieve >90% eCOA/ePRO compliance by engaging patients as active participants in each study. This approach has powered all study sizes, from large-scale virtual studies with over 13,000 participants, all the way down to pediatric rare disease studies with just 60 critical families.

Book a demo

We may process your personal information for carefully considered and specific purposes which are in our legitimate business interests and enable us to enhance the services we provide, but which we believe also benefit you. Click here to learn more about what we mean by legitimate interests, and when we may process your information in this way.

High Compliance

Over 90% compliance in real-world studies

Faster Studies

Reducing study timelines by ⅓

Quality Data

Capturing GCP-compliant data, ready for submission

“We needed an easy-to-use solution, that can be used across multiple countries, to manage a high volume of data capture – uMotif’s platform provides the opportunity to engage our patients”

Professor Pratik Choudhary Project Lead, King’s College London