Deploy eCOA in Clinical Trials

Patient-centered eCOA in clinical trials that delivers high-quality data for all trial phases.

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Patient-first design, combined with regulatory-compliant technology, provides the most modern platform for eCOA in clinical trials.

eCOA in Clinical Trials: Phase I – III

Capturing Patient Reported Outcomes, whether site-based or hybrid, is critical in clinical trials. Questionnaire and visit schedules can be complex and the burden high on both patients and site staff.

From oncology to cardiovascular and from inflammatory to rare disease indications, the uMotif platform’s powerful scheduling, reminders, patient engagement and data capture modules support highly complex global clinical trials.

eCOA in Clinical Trials: Phase IIIb and IV

Later stage clinical trials offer opportunities for sponsors to strengthen their dataset, engage patients and broaden their reach. The uMotif platform provides solutions to capture symptoms, outcomes, eDiaries and other data, while building an engaged patient group.

Available in any language and swiftly configured for global deployment for later phase clinical trials.

Decentralized Clinical Trials

Sponsors continue to carefully consider how elements of their trials can move out of the clinic and into patients’ homes. Decentralization can deliver significant benefits, but must balance high-quality data capture with a patient-centric approach.

Our toolkit of solutions enables sponsors to decentralize, while keeping the patient motivated during the trial.

eCOA/ePRO Solutions For Clinical Trials

Our cloud-based eCOA/ePRO platform, APIs and workflow integrations support the delivery of large-scale clinical trials across the globe. Integrating with other clinical trial technology and services, we achieve high rates of data capture compliance and participant retention.