Overview
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Starting Price
Custom
oomnia Specifications
Appointment Management/Scheduling
Lab Integrations
Customizable Forms
e-Prescriptions
What Is oomnia?
oomnia is a real-time SaaS platform that unifies all essential clinical trial tools-EDC, RTSM, CTMS, eTMF, eCOA, ePRO, and eConsent-into one cohesive system. With single sign-on, users save up to 75% of time spent navigating between systems. Its multi-tenant design allows stakeholders to manage multiple trials on a single instance and gain oversight of entire portfolios. No coding is required due to intuitive drag-and-drop features. oomnia is fully interoperable, eliminating integration issues, and offers role-based access with a user-friendly interface customizable by language and notifications. Real-time reporting, seamless randomization, and complete audit logs enhance efficiency and data accuracy.
oomnia Pricing
The vendor offers custom oomnia price plans to cater to different needs. Request a personalized oomnia pricing quote for your business today!
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
oomnia tools
oomnia offers eight essential, fully interoperable tools for easier clinical study management:
CTMS - Clinical Trial Management System (CTMS) centralizes trial data, tracks sites, manages budgets, monitors visits and automates workflows for better study control.
eCOA - electronic Clinical Outcome Assessment (eCOA) software captures real-time patient data via devices, reducing errors through instant validation, simplifying trial workflows.
eConsent - eConsent supports both digital and paper consent, empowering patient choice and reducing consent time from weeks to minutes.
EDC - Electronic Data Capture (EDC) unifies clinical trial data capture with custom eCRFs, real‑time validation, audit trails and role‑specific dashboards.
ePRO - electronic Patient Reported Outcomes (ePRO) software captures patient data via personal devices for real-time, secure, accurate reporting that boosts clinical data quality.
eSource - eSource software captures real-time clinical trial data from EHRs, wearables, and apps, improving accuracy, speed, and compliance.
eTMF - eTMF system for clinical teams with dashboards, audit trail, role-based access, fast setup, one login for EDC, RTSM, CTMS.
RTSM - Randomization and Trial Supply Management (RTSM) automates patient randomization and tracks trial supply in real time through integrated eCRF, reducing delays and manual errors.
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.
Dashboards 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.
eSource 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.
Web 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.
