We engage patients to capture eCOA / ePRO data.
Patients are at the heart of every study.
We’ve designed our modern technology to put patients at the centre of research, capturing high quality data. Swiftly configured and deployed in any therapy area, our solutions power world-leading research globally from site based to fully decentralized trials.
The uMotif platform includes key modules, configured to the needs of each study including:
eCOA, ePRO and eDiaries
Symptom & drug tracking
Engagement reminders, notifications and alerting
Study scheduling and companion applications
eConsent and informed onboarding
Devices, wearables and home testing
A configurable toolkit for any study, in any language
Every study is different, each requires a tailored solution. As trials become more complex and global we simplify delivery, decentralization and data capture through integrations with our partners.
– IRT and drug supply
– EDC and eSource
– Home Nursing
– Stipends, payments & tailored engagement
– Wearables, Devices and home sampling
– Data tokenization and linkage
eCOA solutions for real world studies
We are true experts in real world patient data capture, having covered all RWE types – including observational research, Long Term Follow Ups, natural history studies, non-interventional trials and registries.
We’ve powered large scale virtual studies with over 13,000 participants, and small-scale paediatric rare disease studies.
Through this deep experience, we understand how engagement in real world studies is critical, where every data point from every participant really matters.
Our unique approach is proven to achieve >90% eCOA / ePRO compliance by engaging patients as active participants in each study.
eCOA solutions for Clinical Trials
From Phase 1 – 3 we deliver GCP-compliant solutions for pharmaceutical and biotech sponsors. Our clinical trial solutions capture eCOA / ePRO and other trial data to the strict requirements of each trial protocol.
We have powered large-scale clinical trials across 30 countries, including China, with provisioned devices for trial participants. Through our 24/7 multilingual helpdesk we support patients and sites globally.
Through our high quality design, trial participants remain engaged, informed and compliant, helping sponsors run fast and effective trials.
We go beyond data capture, offering participants a companion app, rich content including study videos, and opportunities to feed back to sponsors on their engagement with the trial.
High compliance
Over 90% compliance in Real World studies
Faster Studies
Over 90% compliance in Real World studies
Quality Data
Over 90% compliance in Real World studies