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Overview

oomnia is the first true all-in-one clinical trial solution that unifies clinical research and clinical practice by offering all relevant tools like EDC, RTSM, CTMS, eTMF, ePRO, eCOA, eConsent, and eSource as integrative parts of one single system.

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Starting Price
Custom

oomnia Specifications

  • Appointment Management/Scheduling
  • Lab Integrations
  • Customizable Forms
  • e-Prescriptions
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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 data from patients, caregivers, and clinicians, reducing errors with instant validation and streamlining trials.

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

Unified System

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.

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Real Time Reporting

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.

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Interoperability And Data Standards

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.

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Accessibility And Offline Support

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.

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Pros And Cons of oomnia

Pros

  • Unified EDC, CTMS, eTMF, RTSM ecosystem

  • Real-time dashboards and comprehensive study oversight

  • HL7 FHIR interoperability with hospital EHRs

Cons

  • Complex EHR integration needs HL7 mapping

  • Module breadth may exceed simple studies

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Frequently Asked Questions

Does oomnia offer an API?

No, the vendor does not disclose any API availability.

Does oomnia have a mobile app?

No, the software does not have a dedicated mobile app.

What language does oomnia support?

oomnia software offers support in the English language.

What types of pricing plans does oomnia offer?

oomnia offers custom pricing options depending on organizational needs and budget. For a custom oomnia cost, contact us now.

What other apps does oomnia integrate with?

It integrates with EHR and lab systems via HL7 and FHIR, and other digital sources through eSource.

Who are the typical users of oomnia?

Typical users of oomnia work in different industries and sectors, such as pharmaceuticals, biotechnology, medical devices, academic research, contract research organizations, and hospitals.

What level of support does oomnia offer?

Support is available via email, phone, demo requests, and professional assistance services including protocol development, data management, and monitoring.