Clinical Trials.

Clinical knowledge at your fingertips.

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Oomnia Clinical Research.

Oomnia CRIS is a comprehensive solution for managing multinational traditional, decentralized, and synthetic clinical trials, ensuring high data quality while enabling precise process and document management.

We have developed Oomnia CRIS with sponsors, clinical research organizations (CROs), and academia in mind.

Our clinical research approach is built on three pillars.

Software.

Innovative software for planning, conducting, and analysis of clinical and workflow data.

Services.

Complete coverage of services focused on data quality, encompassing all aspects of clinical research operations, from planning to analysis and submission.

Global Capabilities Network.

Integration of real-world data and a comprehensive set of services to run global large-scale clinical trials through the AcrossGlobal Alliance.

Oomnia Clinical Research Information System CRIS.

Oomnia Clinical Research image

Oomnia CRIS is a comprehensive solution for managing multinational, traditional, decentralized, and synthetic clinical trials, ensuring high data quality while enabling precise process and document management.

Checkmark icon Reduce costs by more than 50%.
Checkmark icon Reduce time to market by at least 30%.
Checkmark icon Improve data quality.
Checkmark icon Improve patient outcomes.
EDC.

EDC.

Collect, clean, and review clinical trial data effortlessly.

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ePRO & eCOA.

ePRO & eCOA.

Streamline data collection directly from patients and ensure highest data quality.

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RTSM.

RTSM.

Effortlessly randomize patients and automate Investigational product supply management.

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CTMS.

CTMS.

Oversee and manage your clinical trial effectively and efficiently.

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eTMF.

eTMF.

Digitally capture, manage, share, and store essential documents and content.

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eConsent.

eConsent.

Improve patient information and consent considering literacy and cultural diversity.

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Medical Coding.

Medical Coding.

Directly assign medical codes in the eCRF in the data collection stage already.

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Safety.

Safety.

Monitor product post approval performance and automate adverse event management.

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Lab Management.

Lab Management.

Centralize laboratory and reference range management and data collection.

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Imaging.

Imaging.

Collect image assessment results directly in eCRF, integrated in the analytical data set.

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Query Management.

Query Management.

Streamline query management and enhance data quality.

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eSource.

eSource.

Enable electronic data capturing on the spot, monitor data entry, and store data in real-time.

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eArchive.

eArchive.

Curate and store your data along the entire clinical trial process life cycle.

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Medical Device Integration.

Medical Device Integration.

Manage pilot studies, pivotal studies and post market follow ups in one system and ensure compliance (EU MDR).

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Services

Oomnia Clinical Research image

We provide comprehensive support and guidance, from identification of requirements, to protocol development, data management, statistical analysis, and medical writing to ensure your success.

Checkmark icon Greater efficiency.
Checkmark icon Higher accuracy.
Checkmark icon True transparency.
Checkmark icon Customer success.

Clinical Trial Professional Services.

Consultation.

Consultation.

Customize your consultation services according to your clinical trial and business needs.

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Data Management.

Data Management.

Generation of high-quality, reliable, and statistically sound data on which to draw your conclusion.

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Pharmacovigilance.

Pharmacovigilance.

Effortlessly manage adverse events to bolster patient safety and improve treatments.

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Biostatistics.

Biostatistics.

Unlock the true potential of your clinical trial data with accurate analyses and presentation.

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Medical Writing.

Medical Writing.

Let our PhD-level experts accelerate your trial to final submission-ready documents.

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Oomnia CRIS Customer Success.

Advisory and Scoping

Advisory and Scoping

We tailor your clinical trial to your needs and scope Oomnia to optimally support your goals.

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Implementation

Implementation

We set up Oomnia according to your requirements and connect all systems.

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Training

Training

We ensure your team is provided with sufficient training from experts throughout the clinical trial.

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Support

Support

We provide 24/7 support to ensure our client and user needs are met.

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Global Capabilities Network.

Global Capabilities Network image

We provide integration of real-world data as well as a comprehensive set of services to run global, large-scale clinical trials through the AcrossGlobal Alliance network.

Checkmark icon Unlimited possibilities.
Checkmark icon Global reach.
Checkmark icon Unique solutions.
Checkmark icon Unique results.
Real-World
Data

Real-World
Data

Streamline your clinical trial document management.

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Experience unique functionality that will change your world.

Interoperability icon

Interoperability

All solutions are semantically inter-operable and ensure seamless data exchange with other internal and external systems.

Reusability icon

Reusability

Each created object is available to you at any time and can be used again, even in other studies.

Flexibility icon

Flexibility

The system is uniquely flexible and can be easily adapted to your changing needs, even in an ongoing study and without downtime.

Compatibility icon

Compatibility

The CDISC standard is integrated into every data field throughout the entire process, starting with the very first data entry already.

Uniqueness icon

Uniqueness

RTSM and centralized laboratory management are integrated in eCRF together with partial date handling.

Generate prolific insights from your clinical trials with a truly interoperable platform.

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