Oomnia unifies EDC, CTMS, eTMF, RTSM, ePRO/eCOA, eConsent, and eSource with real-time reporting and HL7 FHIR links. While it may exceed needs for smaller studies, its strong security, audit trails, and offline access make it a solid choice for regulated teams.
oomnia Specifications
Appointment Management/Scheduling
Lab Integrations
Customizable Forms
e-Prescriptions
What Is oomnia?
oomnia is a cloud-based clinical trial management platform designed for sponsors, contract research organizations, and research sites. It centralizes processes through modules such as electronic data capture (EDC), clinical trial management system (CTMS), and electronic trial master file (eTMF). With real-time reporting dashboards, teams gain immediate visibility into enrollment and monitoring. Offline-ready access ensures continuity in low-connectivity environments, while compliance-focused audit trails support regulatory standards, helping streamline trial oversight, reduce errors, and maintain data integrity throughout studies.
oomnia Pricing
oomnia Integrations
Who Is oomnia For?
oomnia is ideal for a wide range of industries and sectors, including:
- Pharmaceuticals
- Biotechnology
- Medical devices
- Academic research
- Contract research organizations
- Hospitals
Is oomnia Right For You?
oomnia may be the right fit if your organization requires a unified platform to manage complex clinical trials with compliance at its core. Its standout features include real-time reporting, offline-ready access, and HL7/FHIR interoperability, which reduce manual errors and strengthen oversight. Certifications such as ISO 27001 ensure data security, making it reliable for sponsors, contract research organizations, and research sites conducting regulated studies.
Still doubtful if oomnia is the right fit for you? Connect with our customer support staff at (661) 384-7070 for further guidance.
oomnia Features
Within one environment, oomnia links EDC, CTMS, eTMF, RTSM, ePRO/eCOA, eConsent, and eSource so data flows instantly between study startup, conduct, and closeout. This reduces manual reconciliation and supports audit readiness with complete trails across modules. These oomnia features cut context switching and maintain a single source of truth.
See How It WorksDashboards consolidate data from sites, patients, and monitoring into a consistent, analysis ready store. Teams view enrollment, queries, deviations, and safety indicators as they happen, then adapt protocols or resources quickly. Real time visibility shortens issue resolution and supports continuous oversight without waiting for periodic extracts or offline collation.
See How It WorkseSource capabilities connect hospital systems and external data sources using HL7 and FHIR. Common Data Elements and templated forms enable reuse across studies, improving consistency and accelerating database setup. Standardized exchange reduces mapping effort, while integrated flows minimize errors when importing labs, visits, and other structured clinical information.
See How It WorksWeb access on any device keeps investigators and coordinators productive during travel, site visits, or remote work. Offline capture covers low connectivity settings, with activity logs and audit trails preserving accountability. Role based permissions control visibility, so stakeholders collaborate securely while maintaining data integrity and regulatory compliance.
See How It Works
