Whether it is investigator-initiated study, observational study, phase 0, 1, 2, 3, or 4 post-market trials, real-world evidence generation to supplement your randomized controlled clinical trial, maximizing the speed of patient enrollment is the proven way to minimize your risk.
With bi-directional communications, scheduling, eligibility screening, and remote touch-less electronic informed consent, investigators can rapidly enroll participants in clinical studies with participants safely reviewing the study material at their own convenience remotely from their own mobile device.
We understand technology is a means to an end. We strive to achieve the right balance between the use of technology and expert human intervention to optimize trial operations. Clinical study teams spend hundreds of hours coordinating participants' schedules to ensure quality and compliance.
Jeeva SaaS streamlines the workflows for eligibility screening, bi-directional communications, and remote electronic informed consents with a focus on accelerating timelines while improving the user experience. We focus on optimizing the study operations so you can focus on research outcomes.
Ready to Explore Jeeva eClinical Cloud for Your Study?
Jeeva eClinical Cloud modules and packages are designed to be disease-agnostic, device-agnostic, flexible, and modular to support patient-preferred decentralized or hybrid trial operations. Schedule a 30-minute call today to determine the fit. We will help you identify technology or protocol complexity gaps to enable an informed decision
