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.

Our eCOA/ePRO platform is designed for patients first to power 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.

eCOA solutions for clinical trials
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High Compliance

Over 90% compliance in real-world studies

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Faster Studies

Reducing study timelines by ⅓

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Quality Data

Capturing GCP-compliant data, ready for submission


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“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

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