Product Overview
Improved Data Quality and Boost Efficiency: Electronic Clinical Outcomes Assessment (eCOA) provides a more accurate reflection of patient outcomes. The reports help researchers identify trends and patterns in patient responses that are not readily visible when data is collected through paper forms.
Reduces Subject Burden: By automating data collection, the Electronic Clinical Outcomes Assessment (eCOA) system reduces the burden on subjects and allows them to focus on their health and well-being rather than on completing cumbersome paperwork.
Increased Efficiency: Our Electronic Clinical Outcomes Assessment (eCOA) solution allows researchers to quickly and easily collect data from multiple sources, reducing the time and resources needed for data collection.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
Cost Effective and Improved Patient Retention: By reducing the need for manual data entry, the Electronic Clinical Outcomes Assessment (eCOA) module reduces administrative costs for researchers.
Minimize Errors and Omissions: They are less prone to errors and omissions, and data is automatically captured, validated, and stored in a secure system. Additionally, they can also be used to collect data on a variety of outcomes.
Jeeva eCOA Software Platform Highlights
Electronic clinical outcomes assessments (eCOA) and electronic patient-reported outcomes (ePRO) are electronic systems used in healthcare and clinical research.
Our eCOA solution enables research investigators to accurately capture clinician-reported outcomes (ClinRO), patient-reported outcomes (ePRO), observer-reported outcomes (ObsRO), and performance outcomes (PerfO) electronically. The module includes a range of tools such as questionnaires, diaries, and surveys completed by patients regularly to assess the impact of a medical condition or treatment on the patient’s health and well-being.
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.