List of Jeeva EDC Software Customers
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Since 2010, our global team of researchers has been studying Jeeva EDC Software customers around the world, aggregating massive amounts of data points that form the basis of our forecast assumptions and perhaps the rise and fall of certain vendors and their products on a quarterly basis.
Each quarter our research team identifies companies that have purchased Jeeva EDC Software for Intelligent Document Processing from public (Press Releases, Customer References, Testimonials, Case Studies and Success Stories) and proprietary sources, including the customer size, industry, location, implementation status, partner involvement, LOB Key Stakeholders and related IT decision-makers contact details.
Companies using Jeeva EDC Software for Intelligent Document Processing include: Immunoact, a India based Life Sciences organisation with 150 employees and revenues of $8.0 million, Farmacon Global, a United States based Life Sciences organisation with 20 employees and revenues of $3.0 million, Frantz Viral Therapeutics, a United States based Life Sciences organisation with 10 employees and revenues of $1.0 million and many others.
Contact us if you need a completed and verified list of companies using Jeeva EDC Software, including the breakdown by industry (21 Verticals), Geography (Region, Country, State, City), Company Size (Revenue, Employees, Asset) and related IT Decision Makers, Key Stakeholders, business and technology executives responsible for the software purchases.
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| Logo | Customer | Industry | Empl. | Revenue | Country | Vendor | Application | Category | When | SI | Insight |
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Farmacon Global | Life Sciences | 20 | $3M | United States | Jeeva Clinical Trials | Jeeva EDC Software | Intelligent Document Processing | 2022 | n/a |
In 2022, Farmacon Global implemented Jeeva EDC Software to enable Hispanic/Latinx and Latin America site engagement for rare-disease and other clinical trials. The deployment emphasized Intelligent Document Processing capabilities to streamline consent documentation and patient-facing materials across multi-center studies.
The implementation used Jeeva EDC Software with explicit use of Jeeva eConsent and patient engagement modules, configured to support electronic case report forms and consent workflows typical of clinical research operations. Configuration work focused on multilingual consent flows and decentralized trial support, aligning electronic data capture and patient interaction features with site-level recruitment and enrollment processes.
Operational scope covered clinical research operations across sites targeting Hispanic/Latinx populations in the United States and Latin America, with an implementation publicized in 2022 and estimated completed that year. Governance centered on study-level configuration of consent and engagement workflows, and reported outcomes included improved eConsent capture, enhanced patient recruitment, and strengthened decentralized trial support in the region.
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Frantz Viral Therapeutics | Life Sciences | 10 | $1M | United States | Jeeva Clinical Trials | Jeeva EDC Software | Intelligent Document Processing | 2022 | n/a |
In 2022, Frantz Viral Therapeutics selected Jeeva EDC Software as part of Jeeva's eClinical platform to execute a multi-site Phase 2 clinical trial for HPV-associated anal HSIL. The implementation centralized eConsent and data capture across US sites and focused on Jeeva EDC Software capabilities categorized as Intelligent Document Processing.
Configuration work emphasized EDC case report form design, electronic consent workflows, and CTMS study planning and site management capabilities within Jeeva EDC Software. Standard EDC activities inferred from the vendor release, such as metadata-driven CRF build, query management, role based access controls, and electronic source documentation workflows, were configured to align clinical operations with remote monitoring needs.
Operational scope extended to clinical operations, site coordinators, study monitors, and regulatory oversight across participating US sites, with the platform used for enrollment tracking and centralized data aggregation. The source material does not specify external system integrations, so initial data orchestration and document processing remained within Jeeva's eClinical platform during the estimated go live.
The selection and publication occurred in 2022, with an estimated go live the same year. Governance changes included updates to standard operating procedures for eConsent and site onboarding, and adjustments to monitoring and data review workflows to reflect centralized electronic capture. The deployment was undertaken to improve recruitment and study operations across US sites, leveraging Jeeva EDC Software Intelligent Document Processing capabilities for clinical data capture and consent management.
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Immunoact | Life Sciences | 150 | $8M | India | Jeeva Clinical Trials | Jeeva EDC Software | Intelligent Document Processing | 2022 | n/a |
In 2022 Immunoact partnered with Jeeva Clinical Trials to deploy Jeeva EDC Software, using the Intelligent Document Processing application to store and share regulatory compliant clinical trial records for cell and gene therapy studies across multi center sites in India. The collaboration was publicly announced in 2022 and the deployment was estimated the same year, enabling Immunoact to avoid building a large in house IT platform while accelerating clinical development timelines.
Implementation centered on core electronic data capture and study management capabilities, with inferred use of EDC and CTMS modules and likely support for eConsent and eCOA consistent with Jeeva EDC Software capabilities. The solution provided centralized regulatory compliant storage, structured document processing, and study level governance controls to support clinical operations, data management, and regulatory submissions for site networks in India. Workflows were reoriented toward centralized data capture and controlled data sharing across investigators and sponsors, with audit trail and access control features implied by regulatory compliance requirements and by the Intelligent Document Processing category.
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