Modern eCOA/ePRO platform powering real-world studies

See how our flexible solutions engage, encourage, and retain patients.

Our unparalleled patient engagement capabilities accelerate real-world data capture, transforming the quality and accuracy of results in real-world studies across the globe.

At uMotif, we understand that success in real-world evidence studies lies in the ability to adapt to diverse study types, settings, and goals.

Our flexible and configurable technology empowers sponsors, CROs, and partners to engage patients, fostering retention and participation in real-world research.

From non-interventional studies to compassionate use programs, uMotif has a strong track of achieving 90%+ compliance with thousands of participants across all real-world study types.

Real-world study perspectives

Insight into how we regularly exceed data capture expectations.

  • Mick's story header

    Hear from a patient behind the research

    Mick shares how using the uMotif app as part of the 100 for Parkinson’s research project made him feel more motivated to participate in the study and empowered in managing his condition.

    Watch video
  • Cloudy with a chance of pain logo

    Case Study: Chronic Pain | Cloudy With a Chance of Pain

    Learn how the uMotif eCOA/ePRO platform helped researchers decode the connection between pain and weather.

    Read case study
  • Blog header - man looking at smartphone

    Blog: Using patient experience data in real-world studies

    Patient insights are expected to become increasingly instrumental in optimizing medicine development and regulatory decision making. Julia Lakeland weighs in on the implications for eCOA/ePRO.

    Read blog

“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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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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