Engaging patients to capture high quality eCOA/ePRO data.
Our next generation technology puts patients at the center of clinical, post-marketing and real-world research. Swiftly deployed in any therapy area, our solutions power world-leading research globally from site-based to fully decentralized trials.
Configured to the needs of each study, key modules in the uMotif platform include:
eCOA, ePRO and eDiaries
Symptom and drug tracking
Engagement notifications and alerts
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 requires a tailored solution. As trials become more complex we simplify delivery and data capture through integrations with our partners:
- IRT and drug supply
- EDC and eSource
- Home nursing
- Stipends, payments and tailored engagement
- Wearables, devices and home sampling
- Data tokenization and linkage
eCOA solutions for real-world studies
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
From phase I – III 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. Our 24/7 multilingual helpdesk supports patients and sites globally.
uMotif’s unique consumer-level design ensures 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 engagement with the trial.
High Compliance
Over 90% compliance in real-world studies
Faster Studies
Reducing study timelines by ⅓
