Seamless Collaboration. Efficient Clinical Trials Unify teams, enhance communication, and speed up clinical trials.
Seamless Collaboration. Efficient Clinical Trials Unify teams, enhance communication, and speed up clinical trials.
Smooth Collaboration for Faster Clinical Trial Success
Collaboration in clinical trials depends on stakeholders receiving the right information exactly when it is collected.
oomnia unifies teams and streamlines communication across clinical trial levels, including sponsors, CROs, site staff, and data management. oomnia provides all stakeholders a single access point for all data and insights, eliminating manual processes and enhancing transparency, leading to faster decision-making. oomnia inherently removes barriers to communication and collaboration by giving everyone access to exactly the information they need when they need it.
Eliminate pain points and decrease costs by ensuring flawless cross functional collaboration.
Simplify Teamwork & Accelerate Trial Progress with a Single Unified Source of Truth
Ensure Smooth Collaboration
Eliminate communication barriers and streamline teamwork across all stakeholders with oomnia.
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Unify teams, streamline communication, and share data effortlessly across all stakeholders.
oomnia offers robust collaboration tools that streamline communication, data sharing, and workflow management. With features like real-time access to a single source of truth, regardless of the type of data, and automatic event notifications, all stakeholders remain aligned and informed throughout the entire clinical trial process. This enables faster decision-making and more efficient operations.
All trial dependent data and processes within a single source of truth.
oomnia streamlines collaboration with the ability to present and analyze data, as well as notify stakeholders of important events, all in real time. By unifying all data capture as well as the eTMF into a single, easy-to-access platform, we enable trial teams to have all the information they need to make decisions and adjustments in real time. Whether you’re coordinating with CROs, Sponsors, or clinical sites, oomnia keeps all stakeholders informed and aligned.
Collect all data, which normally has been collected in disparate systems, in one place. This includes participant data, protocol deviations, monitoring visits reports, randomization, and trial supply.
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.
Stay connected and informed with instant access to critical trial data. With oomnia, collaboration is flawless as all stakeholders can access, review, and analyze real-time clinical trial data from anywhere at any time. Whether monitoring patient recruitment or site performance, oomnia live dashboards ensure transparency and data accuracy, enabling informed decision-making at every stage. Automated notifications and alerts keep teams updated on key trial events, ensuring timely responses and a smooth trial process.
Ensure all stakeholders are working with the most up-to-date data, including patient recruitment numbers, site performance, and trial progress.
Safeguard your data with confidence and meet the most rigorous standards oomnia is designed to ensure your clinical trial data adheres to the highest global regulatory standards, including ICH GCP, 21 CRF Part 11, and EU Annex 11. Our software incorporates comprehensive audit trails for all EDC documents and modules, as well as a detailed event log of all activities by all system users, regardless of role. Wemedoo complies with ISO 27001:2022 and follows GAMP5 software development processes, while all features and releases are extensively pre-validated by our team. With our software and procedures you can trust that your trial data is secure and adheres to the highest regulatory requirements.
Ensure all stakeholders are working with the most up-to-date data, including patient recruitment numbers, site performance, 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
Infinite scalability with oomnia empowers your clinical research teams to expand operations without limits. By providing seamless adaptability to any number of trials, regardless of their size or complexity, your teams can focus on groundbreaking research without worrying about technical constraints. With built-in flexibility and professional support, you can confidently scale your trials, ensuring smooth operations, increased efficiency, and optimized outcomes.
Advanced security measures protect your data from breaches and leakage, allowing your team to focus on driving research forward without worrying about data security.
Effortlessly stay compliant with global and local regulations, as well as the latest industry guidelines in all aspects of data security.
Even in the face of disruptions, continuous monitoring, rapid recovery systems, and automated backups ensure minimal downtime and smooth operations, keeping your trials running without interruption.
