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 losing a child to a rare congenital disorder and a brother to a chronic disease, Dr. Harsha Rajasimha took action. As the founder and CEO of Jeeva, he applied his postdoctoral training at the NIH and FDA, along with his industry experience, to improve access to treatments for rare and chronic diseases. His mission: eliminate clinical trial bottlenecks and accelerate research.
Jeeva partners with sponsors to run modern clinical trials with greater efficiency and lower costs. Its unified platform replaces multiple point solutions and vendors with one secure, streamlined system. With a single login, users gain access to real-time data, monitoring dashboards, and an intuitive digital patient portal.
The platform enhances efficiency for all stakeholders—patients, coordinators, and investigators—by automating repetitive tasks through AI and a patient-first technology stack.
