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Why oomnia

oomnia accelerates academic clinical trials with a powerful, secure clinical research information system.

Free License for Academic Researchers

The free usage of oomnia is our contribution to your research. Work on the fly with oomnia and boost your academic study.

Seamless Multicenter Collaboration

Effortlessly coordinate studies across multiple research centers, and improve communication and data consistency.

Built-In Compliance & Security

Stay compliant with regulations (GCP, GDPR, FDA 21 CFR Part 11) through automated workflows and secure data handling.

Real-Time Insights

Instantly track trial progress, monitor data quality, and make timely, informed decisions.

Unified Platform

Integrate multiple clinical data management tools into a single intuitive system and reduce complexity.

AI-Enhanced Workflows

Real-time data flow between Hospital Information Systems (HIS) and Electronic Data Capture (EDC) streamlines workflows and enhances productivity.

What Academic Researchers Value Most in oomnia

Academic institutions tell us oomnia provides capabilities that far exceed their initial expectations. Here's how our platform delivers unique added value:

Flexible and Scalable for All Study Sizes

Whether running small pilot projects or large-scale international studies, oomnia scales effortlessly to meet your requirements without added complexity or cost.

Interoperability and Data Reusability

Easily integrate with existing systems such as Electronic Health Records (EHRs), laboratory information systems, and biobanks, ensuring your data remains interconnected and reusable across future studies.

Automated Reporting & Data Quality Assurance

Built-in reporting tools streamline mandatory documentation, audits, and publication submissions, while intelligent algorithms continuously ensure your data meets the highest quality standards.

Dedicated Academic Support

Benefit from our specialized support for academia, offering focused guidance and assistance tailored to the unique needs and challenges faced by academic researchers.

Explore All oomnia Features

oomnia offers eight essential, fully interoperable tools for easier clinical study management. Integrate seamlessly with existing systems, use only what you need, and capture real-time data from multiple digital sources.

EDC

RTSM

eTMF

CTMS

eConsent

ePro

eCOA

eSource

Our Contribution to Advancing Academic Research

We have listened closely to academic researchers and institutions, carefully gathering their key requirements and expectations for clinical research platforms. Not only have we addressed these requirements, but we have consistently exceeded them. Now, we want to share these insights and solutions with the broader academic community to help accelerate your research.

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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

Features of oomnia for academia

Dive more deeply into all the functions academic research needs.

Our system covers everything essential for academic studies, ensuring a comprehensive approach to clinical data management. The user-friendly data entry, thorough monitoring, and advanced statistical capabilities enhance your research process. With regulatory compliance and a reliable supplier profile, our solution meets the diverse needs of academic researchers. Discover more functions in the following eight categories.