Clinical Trials.
Clinical knowledge at your fingertips.
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 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.
Reduce costs by more than 50%.
Reduce time to market by at least 30%.
Improve data quality.
Improve patient outcomes.
ePRO & eCOA.
Streamline data collection directly from patients and ensure highest data quality.
Learn MoreRTSM.
Effortlessly randomize patients and automate Investigational product supply management.
Learn MoreeConsent.
Improve patient information and consent considering literacy and cultural diversity.
Learn MoreMedical Coding.
Directly assign medical codes in the eCRF in the data collection stage already.
Learn MoreLab Management.
Centralize laboratory and reference range management and data collection.
Learn MoreImaging.
Collect image assessment results directly in eCRF, integrated in the analytical data set.
Learn MoreeSource.
Enable electronic data capturing on the spot, monitor data entry, and store data in real-time.
Learn MoreMedical Device Integration.
Manage pilot studies, pivotal studies and post market follow ups in one system and ensure compliance (EU MDR).
Learn MoreServices
We provide comprehensive support and guidance, from identification of requirements, to protocol development, data management, statistical analysis, and medical writing to ensure your success.
Greater efficiency.
Higher accuracy.
True transparency.
Customer success.
Clinical Trial Professional Services.
Consultation.
Customize your consultation services according to your clinical trial and business needs.
Learn MoreData Management.
Generation of high-quality, reliable, and statistically sound data on which to draw your conclusion.
Learn MorePharmacovigilance.
Effortlessly manage adverse events to bolster patient safety and improve treatments.
Learn MoreBiostatistics.
Unlock the true potential of your clinical trial data with accurate analyses and presentation.
Learn MoreMedical Writing.
Let our PhD-level experts accelerate your trial to final submission-ready documents.
Learn MoreOomnia CRIS Customer Success.
Advisory and Scoping
We tailor your clinical trial to your needs and scope Oomnia to optimally support your goals.
Learn MoreTraining
We ensure your team is provided with sufficient training from experts throughout the clinical trial.
Learn More
Experience unique functionality that will change your world.
Interoperability
All solutions are semantically inter-operable and ensure seamless data exchange with other internal and external systems.
Reusability
Each created object is available to you at any time and can be used again, even in other studies.
Flexibility
The system is uniquely flexible and can be easily adapted to your changing needs, even in an ongoing study and without downtime.
Compatibility
The CDISC standard is integrated into every data field throughout the entire process, starting with the very first data entry already.
Uniqueness
RTSM and centralized laboratory management are integrated in eCRF together with partial date handling.
