Description
Jeeva's virtual control room empowers biopharma and medical device sponsors to oversee clinical trials from start to finish with real-time monitoring, improving efficiency, minimizing risks, and reducing costs—all via a single login and subscription model. The platform significantly eases logistical burdens for both participants and study teams, offering features such as bi-directional communication, eligibility screening, scheduling, electronic data capture (EDC software), electronic clinical outcome assessments (eCOA), TeleVisits, and remote touchless electronic informed consent.
Powered by AI, Jeeva automates visit scheduling and protocol configurations, seamlessly integrating modules for eConsent, ePRO/eCOA/EDC, TeleVisits/VideoVisits, and adverse event tracking with MedDRA coding. It also includes a patient engagement portal with SMS, email, audio, and video communication, as well as reminders and notifications to enhance trial participation and engagement.
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