UNIPHI.io

UNIPHI.io believes increased data capture flexibility is not enough to confidently deliver on highly complex clinical trials. We must use technology to assist every individual : sites, patients, monitors, and sponsors/CROs, working on a clinical trial with the simple concept of “What do I do next?”. Our clinical data platform developed for the capture, display, and management of evidence data captured from and about patients in compliance with the protocol and study conduct. Users can rely on their own familiar devices: tablet, smartphone, PC/laptop with any browser. Formatting scales to device screen size automatically. Free-text when required uses the local browser language The eSource platform supports EDC/eCRF, eConsent, eCOA, connected devices, data integration, IRT/RTSM, study oversight and project management. The UNIPHI.io platform is a collaborative tool allowing project team members to work together in real time. Quick and easy low-code/no-code configuration: form creation/revisions are stored centrally based on agreed design, including content, order of presentation, scheduling, etc. Content is adaptive: our platform uses stored and current information to enhance site and patient choices at the moment and in the future. Workflow management is intelligent. Project/study management is facilitated by logical notifications and tasks based on roles, the dynamic rule engine and event schedules. Deliverables: Easy to use system to capture and manage evidence about how patients feel and function

网站

https://www.uniphi.io/

UNIPHI.io 的外部链接

所属行业

研究服务

规模

11-50 人

总部

Boston，Massachusetts

类型

私人持股

创立

2018

领域

Clinical Outcomes、eConsent、eCRF、Data Monitoring tools、Patient Focused Drug Development、Decentralized Hybrid Clinical Trials、eTMF和RTSM