Delivering high-quality endpoint data for late phase clinical studies
Book a demo of uMotif’s eCOA/ePRO platform to see how we power unparalleled levels of patient engagement that can transform the speed, accuracy and quality of data in your next late phase study

Our modern eCOA/ePRO engagement platform offers solutions for high-quality late phase clinical trials.
Late phase IIIb and IV clinical trials are crucial for gathering real-world evidence. uMotif’s unique eCOA/ePRO platform is flexible to meet the requirements all types of late phase clinical trials from virtual to site-based studies.
Uniquely designed with patients, for patients, our platform helps reduce the burden of study participation to drive high levels of patient participation and compliance, in every study.
Available in any language and swiftly configured for global deployment for late phase clinical trials, uMotif’s validated platform supports the delivery of large-scale late phase trials across the globe. We achieve high rates of data capture and participant compliance and retention that often far exceeds our customers’ expectations.

Late Phase Insights
Insights from our late phase patient engagement experts
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The ever changing patient burden and decentralized clinical trials
In this podcast by Note to File, Steve discusses the state of ePRO/eCOA, the ever changing patient burden and decentralized clinical trials.
Listen to Podcast -
Case Study: Papworth Hospital Cardiac Rehabilitation
Papworth Hospital boosts cardiac rehab program outcomes and efficiency with uMotif eCOA/ePRO platform.
Read case study -
Article: Engaging patients with behavioral science and patient-centered technology
Engaging patients with behavioral science and patient-centered technology
Find out more
“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

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
Trusted by leading companies
across the globe:
