Jeeva's virtual control room empowers biopharma and medical device sponsors to conduct modern clinical trials with real-time monitoring, enhancing efficiency, reducing risks, and cutting costs through a single-login, single-subscription model. This platform significantly eases the logistical challenges for both participants and study teams with features like bi-directional communication, eligibility screening, scheduling, electronic data capture (EDC), electronic clinical outcome assessments (eCOA), telehealth visits, and remote, touchless electronic informed consent. The AI-driven Jeeva platform streamlines and centralizes visit scheduling and protocol configuration, mapping them to various modules. These modules encompass eConsent, ePRO/eCOA/EDC, telehealth/video visits, adverse event capture with MedDRA coding, and a patient engagement portal that supports SMS, email, audio, and video communications, along with reminders and notifications.