Jeeva Informatics Solutions Inc.
4 software found

Jeeva Informatics Solutions Inc. software

Jeeva - Scalable Modular SaaS Software for Clinical Trials

Jeeva`s patent-pending modular solution is designed from the ground up on the most powerful cloud platform with one login from any browser-enabled mobile device for remote patient screening, education, enrollment, electronic informed consent, bi-directional communications via video calling, telemedicine, SMS, email, and evidence generation including electronic patient-reported outcomes and clinical outcomes assessments, with a modern user experience.

Jeeva - Accelerate Patient Enrollment Software Tool

Patient recruitment is a major barrier in clinical trials. This involves identification of patients and then enrolling eligible patients into the trial. This requires a all-in-one tool that brings together remote eligibility screening, omnichannel patient engagement for patient education, multimedia information exchange, and remote electronic informed consent.

Jeeva - SaaS-Based Collaboration Platform Software

Clinical research sites, sponsors, and CROs, minimize the logistical burdens of the informed consent process on a per-clinical-trial subscription or enterprise license. The modular subscription service is based on number of patients and can scale with the study enrollment process. Automate the manual repetitive tasks of explaining the study protocol, risks, benefits, samples or data use, and answering frequently asked questions. We heard you. eCaaS is our solution!

Jeeva - Subscription Service Modular Software

Clinical research sites, sponsors, and CROs, minimize the logistical burdens of paper based process for gathering patient reported outcomes, patient diaries, patient satisfaction, and quality of life questionnaires. Whether standardized or custom on a per-clinical-trial subscription or enterprise license. The modular subscription service is based on number of patients and can scale as the study enrollment progresses. The Jeeva™ ePRO solution enables cohort studies, patient registries, natural history studies, biobanking, clinical research, or clinical trials.