Product Overview
Waste of Research Investigator’s Time: A research investigator spends an average of 15-60 minutes per subject to obtain proper informed consent. The process is very repetitive.
Overload of Information for Patients in 15min: Patients are overwhelmed by the enormous amount of information they are expected to read and understand before they decide and provide informed consent in a single consultation. Patients can’t consume ~50 pages in 15 min.
Cost Associated with In-person Informed Consent: The direct and indirect costs of obtaining informed consent include investigator time, coordinators, nurses, and facilities.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
Huge Logistical Burdens: Patients or caregivers and legally authorized representatives often have to travel in person to the investigation site and wait for several minutes to hours to complete and access proper informed consent.
Patient Comprehension: Investigators are required to verify that the patients or caregivers fully understand the risks and benefits of participating in a clinical trial before obtaining informed consent.
No Support for Various Scenarios: Modern clinical trials require flexible scenarios for obtaining informed consent in-person or remotely at multiple sites nationally or globally. There is a lack of flexible tools for all scenarios.
About the company
After suffering the loss of a child to a rare congenital disorder and a brother to a chronic disease, Jeeva founder and CEO Dr. Harsha Rajasimha decided to apply his years of postdoctoral training at the National Institutes of Health and the U.S. Food and Drug Administration, as well as his work in the healthcare and life science industry, to accelerating access to treatments for rare & chronic diseases by eliminating bottlenecks in the clinical trials process.
Jeeva partners with clinical research sponsors to execute modern clinical trials with significant efficiency and cut costs using their innovative one-login unified software platform for end-to-end study execution. Jeeva eliminates the need for numerous point solutions and vendors, boosts efficiency for all users, a digital patient engagement portal, with one flat subscription fee solution with one login access to real-time data and monitoring dashboards. Jeeva is driven by AI and tech innovation to automate manual repetitive tasks and was purpose built using modern patient-centric technology stack. Jeeva delivers rapid and complete protocol configuration in 2-4 weeks, remote patient screening, eConsent, referral to investigator sites, randomization, electronic data capture, remote clinical outcomes assessments including patient reported outcomes, eDiaries, televisits or video visits, with a patient engagement portal, appointment booking and rescheduling, and much more under a single login for each stakeholder.
