Jeeva Clinical Trials Inc.

Jeeva’s Schedule of Visits is a step-ahead solution to map all the necessary activities relating to ePRO, eCOA, eCRF, eConsent, eVisit, and other lab procedures.  In addition, it automates validations, protocol deviations, reminders, notifications, form assignments, appointment scheduling, and different user workflows to bring unprecedented efficiencies to trial management. 

To bring the patients and researchers on a single row, Jeeva created a dedicated software that facilitates study teams and patients to conveniently communicate via various channels, such as SMS, email, audio, and video resources.  Additionally, groups and patients can utilize multiple social media platforms, including Facebook, Twitter, Instagram, and WhatsApp, to facilitate patient education, screening, and recruitment. 

Jeeva’s Electronic Patient-Reported Outcomes (ePRO) & Electronic Clinical Outcome Assessments are a one-stop solution to capture questionnaires and diary-based data collection, with scoring or skip logic, reminders, alerts, and notifications and enhance remote patient engagement.  With an easy-to-configure and launch facility, ePRO & eCOA help patients and researchers to share flexible and compliant clinical trial data securely and remotely. 

Jeeva eConsent as a Service (eCaaS) is a customizable and configurable solution that minimizes the logistical burden on patients' and investigators' time by more than 90%, including patient enrollment from multiple channels with flexible add-on features. 

It is a software from Jeeva that aims to reduce manual data entry, saves time and costs, and offers real-time monitoring and highly efficient security features that are valuable to researchers and patients in the clinical trial industry.