oomnia
Transform your clinical trials with oomnia, the all-in-one solution that unifies research and practice for seamless management and efficiency.
oomnia stands out as the pioneering comprehensive solution for clinical trials, seamlessly merging clinical research with clinical practice. It provides a range of essential tools, including EDC, RTSM, CTMS, eTMF, ePRO, eCOA, eConsent, and eSource, all integrated into a singular cohesive platform.
What Is oomnia?
oomnia is a cutting-edge SaaS solution designed to streamline clinical trials by integrating all vital tools such as EDC, RTSM, CTMS, eTMF, eCOA, ePRO, and eConsent into a single platform. With the convenience of single sign-on, users can reduce navigation time between different systems by as much as 75%. Its multi-tenant architecture enables stakeholders to oversee multiple trials within one instance, providing a comprehensive view of their entire portfolio. The platform is user-friendly and requires no coding thanks to its drag-and-drop functionalities. oomnia ensures full interoperability to avoid integration challenges and features role-based access that can be tailored in terms of language and notifications. Enhanced efficiency and data precision are achieved through real-time reporting, smooth randomization processes, and complete audit logs.
oomnia Pricing
The vendor provides tailored pricing plans for oomnia to meet diverse business requirements. Get in touch today to receive a customized pricing quote for your organization!
Who Is oomnia For?
oomnia caters to a variety of sectors and industries, including:
Pharmaceuticals
Biotechnology
Medical devices
Academic research
Contract research organizations
Hospitals
oomnia Tools
oomnia provides eight essential tools that are fully interoperable, facilitating simpler management of clinical studies:
CTMS - The Clinical Trial Management System centralizes trial data, keeps track of sites, manages budgets, monitors visits, and automates workflows for enhanced study oversight.
eCOA - The electronic Clinical Outcome Assessment software gathers real-time data from patients, caregivers, and clinicians. It minimizes errors with immediate validation while streamlining trial processes.
eConsent - This tool supports both digital and paper consent methods, giving patients the power to choose and cutting down consent time from weeks to mere minutes.
EDC - The Electronic Data Capture system integrates clinical trial data collection with custom eCRFs, real-time validation, audit trails, and dashboards tailored to specific roles.
ePRO - The electronic Patient Reported Outcomes software allows patients to report data using their personal devices for secure and accurate real-time reporting that enhances the quality of clinical data.
eSource - This software captures real-time clinical trial data from EHRs, wearables, and applications, boosting accuracy, speed, and compliance.
eTMF - The electronic Trial Master File system offers dashboards, audit trails, role-based access, quick setup, and a single login for EDC, RTSM, and CTMS.
RTSM - Randomization and Trial Supply Management automates patient randomization while tracking trial supplies in real-time through integrated eCRFs to minimize delays and reduce manual errors.