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Superior Data Security for Peace of Mind

Safeguard your Trial Data with Advanced Encryption and Compliance Measures

  • NAdvanced encryption protocols
  • NComprehensive access control
  • NRegulatory compliance assurance

Superior Data Security for Peace of Mind

Safeguard your Trial Data with Advanced Encryption and Compliance Measures

  • NAdvanced encryption protocols
  • NComprehensive access control
  • NRegulatory compliance assurance

Superior Data Security for Clinical Trials

Safeguard your clinical trial data with confidence

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.

Ensure Robust and Reliable Data Security in your Clinical Trials
Protect your trial data with advanced encryption and compliance, giving you peace of mind and full control.
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Immediate benefits of oomnia

Strengthen data security, ensure compliance, and maintain uninterrupted operations

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 life cycle. Wemedoo regularly undergoes external testing and validation of a procedure. As a result, we are an ISO 27001 certified Swiss company, which ensures the highest procedural standards in handling sensitive and proprietary data. From technical aspects, we perform our data operations within a secure environment trusted by numerous global clients.

Ultimate peace
of mind

Advanced security measures protect your data from breaches and leakage, allowing your team to focus on driving research forward without worrying about data security.

Effortless regulatory compliance

Effortlessly stay compliant with global and local regulations, as well as the latest industry guidelines in all aspects of data security.

Uninterrupted
operations

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.
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.

Key Security Features

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.

Secure Data

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.

Data encryption

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oomnia protects trial data with encryption both at rest and in transit, ensuring it remains secure at all times.

Software Development Life Cycle

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Architectural aspects, software development patterns, internal human software testing procedures, and automatic, classical, and AI-based code tests are regularly maintained.

Compliance

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Our infrastructure also allows compliance with globally accepted standards and local rules and regulations. Data can be saved, managed, and backed up within geographical areas required by local laws and regulations.

Granular Access Control for Data Security

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.

Customizable permissions

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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.

Full data access control

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Manage and restrict access to sensitive data effortlessly, ensuring that only authorized personnel can interact with it in accordance with ICH GCP and GDPR guidelines.

Organization based access control

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Quickly set up the trial organizational structure that automatically controls user and role access to all documents, data, and modules across the entire trial.

Two Factor Authentication (2FA)

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Easily enable two factor authentication for each role independently, allowing organizations to ensure robust security for the most sensitive roles, while keeping the overall process light for others.

Compliance and Oversight

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.

Adherence to international regulatory standards

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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 CRF Part 11, and EU Annex 11, ensuring that your clinical trial data meets global security and privacy requirements.

Comprehensive audit trails

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oomnia has built-in comprehensive audit trials for all EDC documents and modules. Audit trials are easily accessible and filterable by any parameter of one's choosing. At the click of a button, track and review user activities and export audit trails for submission to regulatory authorities.

Audit trail review

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Be ahead of the curve with our flexible and fully customizable integrated real-time graphical reporting, which allows for easy mining of audit trail data and metadata from anywhere in the system. This enables the creation of any reports for audit trial reviews, even in real time.

Event logs

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oomnia records all actions by system users in a comprehensive event log. Trust that no matter what actions have been performed, oomnia tracks the who, what, when, and where (the IP address).

See oomnia in action

Explore the full spectrum of our unified clinical trial tools through an insightfull demo call conducted by our esteemed oomnia experts.

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