Real-Time Reporting Real-Time reporting for clinical trial success. Make informed decisions faster with real-time access to critical trial data.
Real-Time Reporting Real-Time reporting for clinical trial success. Make informed decisions faster with real-time access to critical trial data.
Superior Reporting Features
The real-time reporting feature of oomnia provides instant access to critical trial data, helping sponsors, CROs, and academic researchers monitor every phase of the clinical trial process.
Whether tracking patient enrollment, completion, site performance, or overall trial progress, real-time insights empower you to make faster, data-driven decisions that keep your trials running smoothly and on schedule.
Gain Immediate Access to Critical Data for Faster Decisions
Make Faster, Data-Driven Decisions
Get live updates and automated reports for streamlined trial management.
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Stay ahead with real-time insights and reporting tools.
With real-time reporting, you gain immediate access to critical trial metrics, helping you stay informed and in control at every phase. Our platform offers powerful features like live data dashboards, automated reports, and instant notifications from EDC forms, triggered by easy-to-set-up rules. We ensure you can monitor trial performance, address issues proactively, and streamline operations effortlessly.
Get an instant overview of your trial performance with real-time graphical reporting and dashboards.
oomnia provides you with immediate, real-time visibility into the key metrics of your clinical trial. From patient recruitment rates, queries, protocol deviations, IMP supply, site performance, and much more, our intuitive dashboard lets you visualize essential data at a glance.
Visualize the key trial metrics that are important to you. Whether it is recruitment rates, AEs, site performance metrics, PDLs, or the progress of your eTMF, they can all be available in easy to understand graphical reports or dashboards.
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.
Generate accurate, comprehensive reports without manual intervention
Automated reports simplify the reporting process by providing accurate, comprehensive reports without the need for manual input. Reports can be set up to be real-time, or to be automatically updated on an agreed-upon schedule. Reports are always available at the click of a button, eliminating the need for manual report delivery.
Most reports are updated in real time, ensuring the most up-to-date data whenever needed, minimizing delays in decision-making and allowing a current cross-section of the data to be available.
Stay proactive and informed with triggered real-time alerts for key events
Reporting goes beyond presenting data in a visually appealing way. With oomnia, be informed in real time ahead of critical events with instant notifications of key events. Set up event-based alerts for patient screening and enrollment, adverse events, safety events, and much more.
Receive real-time updates on key trial events, ensuring you are informed of important milestones like patient recruitment and trial progress.
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
Our reporting feature offers a range of benefits that empower key stakeholders to manage clinical trials more effectively. With real-time updates and proactive alerts, you can address risks early, ensure accurate data, and keep your trial moving forward smoothly. By providing instant access to critical data, and by automating manual tasks, our platform helps you make informed decisions quickly and keep your studies on track. Discover how real-time reporting can enhance efficiency and ensure the success of your clinical trials.
Make informed decisions quickly with real-time access to trial data, allowing you to address issues immediately and ensure that the trial progresses smoothly.
Automate manual reporting tasks and streamline the process of monitoring trial performance, freeing up resources to focus on high-value activities that improve trial outcomes.
Receive real-time alerts on potential issues, such as low patient recruitment or missed milestones, allowing for proactive management. This allows you to mitigate risks early, avoiding delays and added costs.
