Jeeva’s virtual control room modernizes clinical trials by helping biopharma and medical device sponsors simplify, standardize, and automate operations. Through AI-powered real-time monitoring, sponsors can optimize workflows, mitigate risks, and reduce costs—all through a single-login, single-subscription platform. The platform automates visit scheduling and protocol configurations, reducing logistical burdens for participants and study teams. It standardizes trial processes with eConsent, ePRO/eCOA/EDC, TeleVisits, MedDRA-coded adverse event tracking, and integrated scheduling tools. With a patient-centric approach, Jeeva improves engagement through bi-directional communication, automated SMS/email/audio/video reminders, and remote consent. By streamlining decentralized trials, sponsors can conduct studies faster, more efficiently, and with greater compliance.

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