Superior Data Security Safeguard your trial data with advanced encryption and compliance measures
Superior Data Security Safeguard your trial data with advanced encryption and compliance measures
Superior Data Security for Clinical Trials
oomnia protects your clinical trial data using comprehensive security protocols designed to prevent unauthorized access. Whether you are managing sensitive participant information or critical research data, oomnia ensures your data is secure with industry-standard encryption and customizable access controls.
With continuous security safeguards and automated data checks, you can trust that your data remains protected at every stage of the trial. This allows you to focus on advancing your research, knowing that your trial data is safeguarded by reliable and compliant security measures.
Safeguard Your Clinical Trial Data with Confidence
Ensure Robust & Reliable Data Security
Protect your trial data with advanced encryption and compliance, giving you peace of mind and full control.
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Protect your sensitive data, control access across trials and roles with ease, and ensure compliance with comprehensive oversight at all times.
Safeguard your clinical trial data and maintain compliance with ease. By implementing advanced encryption protocols, customizable access controls, and real-time monitoring, oomnia ensures your data remains secure at every stage of the trial. Whether it is protecting sensitive information or adhering to global compliance standards, oomnia provides a unified solution for data security. With these robust security tools, you can confidently run your clinical trials, knowing that your data is secure and regulatory requirements are met or exceeded.
Information security and data infrastructure are built into our company culture.
Wemedoo provides our customers with a secure and reliable environment supported by state-of-the-art technology accompanied by procedures and various safeguard mechanisms. Professional and process aspects accompany our security technology infrastructure, and there is a clear division of roles and responsibilities. Our security-oriented thinking starts with software conceptualization and development, accompanied by rigorous testing, and spans the whole data management lifecycle.
oomnia protects trial data with encryption both at rest and in transit, ensuring it remains secure at all times.
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.
Control access with fully extensible and customizable permissions
Maintaining tight control over sensitive data is essential in clinical trials, but it can be tricky to set up, especially when running multiple trials, while using RTSM, eTMF, CTMS, ePRO, and more. oomnia provides a simple yet incredibly powerful method of assigning roles and permissions ensuring only authorized personnel can view or modify critical information, significantly reducing the risk of data breaches or data leakage.
Say goodbye to complex role assignments across disparate systems and modules. In our unified system, role based permissions are set in one place and are instantly and seamlessly applied across all modules. This feature ensures that your data governance remains robust, giving you complete oversight and helping your organization adhere to strict security protocols.
Create an indeterminate number of roles, each with their own set of permissions for all modules, as well as EDC and read‑only document types, and personally identifiable information.
oomnia is designed to ensure your clinical trial data adheres to the highest global regulatory standards, including ICH GCP, 21 CFR 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.
Wemedoo is ISO 9001 and ISO 27001 certified, and we have been FDA and Swiss Medic inspected with no findings. Our software complies with critical frameworks such as ICH GCP, 21 CFR Part 11, and EU Annex 11, ensuring that your clinical trial data meets global security and privacy requirements.
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.
