ClinOne features its electronic patient reported outcomes modules which allow patients to bring their own device (BYOD). The technology is an embedded within our ClinTrialConnect module to provide a single central technology between sponsors, research sites, and patients. The technology includes a pre-programmed library of approved, therapeutically-focused validated questionnaires across a broad range of languages.
The validated questionnaires are completed through a patient’s device, or patients may optionally complete their questionnaires upon arrival to their treatment and follow up visits. The technology monitors patients’ compliance and automatically notifies research site members of compliance. ClinOne’s ePRO Lite will provide a digital copy of the PDF questionnaires as well as an export to EDC providers of choice.
