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.
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Sponsors choose Jeeva for our unified and modular eClinical platform, which accelerates trial timelines, enhances real-time oversight, and minimizes vendor management complexity. Whether for single or multi-country studies, Jeeva’s integrated solutions support efficiency and scale while reducing operational risks.
Jeeva seamlessly integrates with your CRO, supplying the technology platform and targeted services to complement the CRO’s operational expertise. Our approach preserves your preferred governance model and allows sponsors to retain control and oversight throughout the clinical trial lifecycle.
Yes, Jeeva is designed for global operations. Our platform features multi-site management, built-in localization for language and regulatory requirements, and standards-based integrations that ensure smooth execution of complex, multi-country studies.
Sponsors benefit from comprehensive, role-based dashboards that deliver real-time insights into enrollment rates, data quality metrics, risk indicators, and financial KPIs. This centralized visibility empowers proactive management and timely decision-making across all your studies.
Jeeva maintains rigorous Computer System Validation (CSV) processes, robust Standard Operating Procedures (SOPs), and consistently prepares inspection-ready documentation. These measures support both routine sponsor audits and regulatory inspections, ensuring ongoing compliance and peace of mind.
Absolutely. Jeeva supports structured migrations with detailed data mapping, parallel system runs for verification, and thorough change management protocols. Our approach minimizes risk and downtime—enabling a seamless transition to modern, unified clinical trial management.
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
