Clinical Research Organisations

By integrating essential tools like EDC, eTMF, RTSM, and CTMS into a unified platform, oomnia reduces redundancies and accelerates processes, allowing CROs to manage trials more efficiently. The real-time data access provided by oomnia enables sponsors to track study progress instantly, facilitating faster, informed decision-making.

Our goal is to eliminate time consuming and costly data reconciliation. Our unified system allows users to enter data only once and for it to be mapped directly to everywhere it needs to be, significantly reducing the risk of data transfer errors. Automatic data validation processes perform real-time checks and our robust audit trails and event logs ensure that the data collected is accurate and valid.

oomnia eases the digital systems compliance burden for Sponsors and CROs by always being current or ahead of FDA, EMA, and ICH regulations. Moreover, the system provides comprehensive audit trails and the possibility of audit trail review (ATR) and visualizations, offering easy access for stakeholders while simplifying audits and inspections for both CROs and sponsors.

A unified approach reduces the need for multiple systems, resulting in lower operating costs for CROs. Our software and best practices can reduce redundant manual labor, thus dramatically increasing efficiency, reducing costs, and making CROs more competitive with Requests for Proposals (RFPs). Our efficient unified system optimizes data collection, randomization and allocation to treatment, as well as planning and monitoring processes, which reduce unnecessary waste and help further cut down expenses.

The collaborative platform of oomnia provides shared access for sponsors, CROs, and study sites, promoting better communication and transparency. Graphical real-time reports and Risk-Based Quality Monitoring capabilities ensure that up-to-date dashboards are always available, keeping sponsors fully informed on progress and issues in real time.

Through our user-friendly ePRO and eCOA solutions, patient compliance is improved, making it easier to engage participants effectively. For example, patients can easily report data through electronic devices such as smartphones, tablets, or web-based platforms, thereby improving data accuracy. Additionally, the simplified eConsent processes enhance participants' understanding of the trial, contributing to higher levels of satisfaction.

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The scalable architecture of oomnia allows CROs to manage studies of any size, from small trials to large, complex projects. A nearly unlimited number of custom visualizations of any type can be implemented and tailored to meet the specific requirements of each study, ensuring flexibility in trial design and management. Tracking study changes is simple and efficient, decreasing downtime and ensuring your project is moving ahead no matter what challenges are being faced.

By leveraging advanced clinical architecture and technology, oomnia positions CROs as industry leaders, offering a competitive edge over others that rely on outdated legacy, or fragmented, systems. The unified nature of the platform enables CROs to stand out, attracting more sponsors by offering streamlined, modern trial management solutions.