Flexible Customization for Enhanced Trial Management
Gives you control over your clinical trials with flexible, out of the box, and easy-to-apply customization. Gone are the days of rigid EDC forms or workflows that have permeated the industry. Whether you need to create custom EDC documents or forms, adjust workflows for specific studies, oomnia enables you to quickly and easily do just that.
oomnia is designed with prevalidated design tools that require no programming knowledge, while allowing for mid-study changes that are as easy as adding a new file, edit check, or workflow. Experience these features in all the oomnia tools, including EDC and CTMS. We streamline your clinical trials by enabling a custom setup for each trial in less time than templated setups on other systems. Combined with quick and easy in-study customization, oomnia ensures that your system is aligned with your research goals at each step, giving you the efficiency and precision required for successful clinical trials.
Personalize Your Trial Processes for Efficiency & Precision
Tailor Your Clinical Trial Management
Customize your trial tools quickly and efficiently with flexible features from oomnia.
BOOK A DEMOCustomize and configure your trials with ease.
Not all trials are the same – in fact, no two trials are the same – so for that reason oomnia provides features that not only enable fast study builds, but custom study builds that are almost as fast as templated forms. Creating custom EDC forms, workflows, or integrated graphical reports is effortless and intuitive. Additionally, easily reuse the forms that do not need customization. This flexibility allows for efficient configurations and ensures your trial workflows fit your research goals perfectly.
Further enhance trial efficiency with reusable templates and personalized forms.
oomnia allows you to create, reuse, and tailor templates to fit your specific trial needs, ensuring a streamlined and efficient trial setup. By using customizable templates and forms across multiple tools, you can save time and ensure consistency across studies, while still meeting the unique requirements of each trial.
Whether you are designing an eCRF, ePRO instrument, SAE Report Form, or any other data collection instrument, our flexible drag-and-drop form designer enables rapid creation of forms and the embedding of workflows tailored to your organization and specific study.
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 reports, notifications, and visualizations to match your trial’s specific needs.
oomnia provides powerful customization options for reporting and visualizing trial data, enabling you to adapt notifications, reports, and dashboards to your exact specifications. This flexibility allows stakeholders to access the most relevant data in real time and make informed decisions faster.
Using multiple Business Intelligence tools, oomnia allows for the creation of any custom report by selecting any data metadata points within or across all system tools. Including EDC documents, RTSM, eTMF, CTMS, ePRO, and much more.
oomnia empowers your clinical trial teams by providing flexible customization tools that enhance efficiency. With the ability to easily create custom eCRFs, EDC forms, reports, and workflows, we help you streamline trial management. This flexibility not only saves time during setup but also ensures that your trial processes are aligned with your specific research goals, allowing for a more effective and tailored approach to clinical trials.
Reduce trial setup times and accelerate research with custom forms and workflows.
Adjust workflows quickly to fit evolving study requirements, ensuring trials remain on track.
Simplify your trial management by adapting workflows to your trial, not the trial to the system.
oomnia - Meeting Industry Standards
Our unified clinical trial software is designed with compliance at its core, meeting critical industry standards. Our commitment to these regulations ensures that your clinical trials are not only efficient but also adhere to the highest levels of data integrity, privacy, and ethical conduct.
21 CFR
PART11
compliant
HIPAA
compliant
GDPR
compliant
ICH GCP
compliant
SWISS DATA PRIVACY LAW
compliant
FAIR ALCOA+
compliant
