Convenient User Interface A convenient user interface for effortless clinical trials. Simplify clinical trial management with an intuitive, streamlined interface.
Convenient User Interface A convenient user interface for effortless clinical trials. Simplify clinical trial management with an intuitive, streamlined interface.
Easily Navigate Your Clinical Trials
Managing clinical trials should not feel like a marathon of endless clicks and complex steps. oomnia is designed to simplify processes for all stakeholders, making clinical research management more intuitive.
Built by clinical research experts, oomnia reduces unnecessary steps and supports efficient trial management. Whether you are a sponsor, CRO, or academic institution, our user-friendly interface ensures a seamless experience, no matter your role within a trial.
Reduce Clicks, Streamline Workflows & Improve Efficiency
Simplify Your Clinical Trials with Intuitive Interface
Streamline workflows, reduce clicks, and enhance productivity in just a few steps.
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Effortless navigation, role-based dashboards, and streamlined workflows for greater efficiency.
oomnia provides clear, streamlined menus and rapid access to essential tools, including EDC, RTSM, eTMF, CTMS, ePRO, eCOA, as well as eConsent. Our software enables simple navigation across all trials and roles, allowing users to easily access relevant data and information. In addition, oomnia reduces manual tasks and automates key processes, ensuring collaboration across teams is fluid and efficient. Together, these features simplify trial management, save time, and improve overall productivity, empowering you to run as many trials as you need with ease and effectiveness.
Navigate easily through clinical trial management tasks. oomnia makes clinical trial management smoother with an organized layout and fewer steps, allowing users to quickly access key tools. Whether managing trial data or reviewing documents, built-in search features and role-based views ensure a user-friendly experience tailored to stakeholders’ needs.
Access key features easily, without overwhelming or complex menus.
Our Proof of Quality
We are ISO 9001 and ISO 27001 certified. Our commitment to robust information security & superior quality management is at the core of our innovative solutions, ensuring reliable & efficient trial management for our clients.
Tailor your reports to focus on the metrics and data that matter most. oomnia provides customizable reporting, allowing users to immediately access the data and metrics most important to their role. With features like customizable layouts, real-time updates, and tailored views, you can easily track KPIs, such as recruitment rates, trial and patient progress, as well as quality metrics. By filtering data, you can easily focus on the most relevant metrics you need, ensuring that you stay informed and in control throughout the trial.
Flexible drag-and-drop form design tools within oomnia EDC for the creation of data capture forms enable easy creation of any EDC forms, regardless of size or complexity.
oomnia optimizes your clinical trial management experience. By streamlining processes and minimizing unnecessary actions, the interface helps you complete tasks faster and more efficiently. The intuitive layout simplifies even the most complex trial workflows, guiding users smoothly through each phase. Tailored specifically for clinical research, the intuitive oomnia interface ensures that every stakeholder can easily navigate and manage trial tasks with confidence and ease.
A streamlined interface helps you save time and effort by minimizing unnecessary actions, allowing you to complete tasks faster. oomnia enhances efficiency by reducing the steps needed for trial setup and management.
Complex trial workflows are made easier to manage with an intuitive layout that guides users through each phase without confusion, supported by real-time monitoring and automated workflows.
Designed by clinical research experts, the interface of oomnia is specifically tailored to the needs of clinical trials, ensuring relevance and usability for all stakeholders.