Overview

Jeeva's virtual control room allows biopharma and medical device sponsors to oversee modern clinical trials from start to finish with real-time monitoring. This enhances efficiency, mitigates risks, and reduces costs—all via a single login and subscription fee. The platform significantly eases logistical hurdles for both participants and study teams, offering features such as bi-directional communication, eligibility screening, scheduling, electronic data capture (EDC), electronic clinical outcome assessments (eCOA), TeleVisits, and remote touchless electronic informed consent. Utilizing AI, Jeeva automates and centralizes visit scheduling and protocol configurations, integrating smoothly with modules for eConsent, ePRO/eCOA/EDC, TeleVisits/VideoVisits, and adverse event capture with MedDRA coding. Additionally, it includes a patient engagement portal that supports SMS, email, audio, and video communications, along with reminders and notifications.