Clinical Trials
Clinical insights at your fingertips
Wemedoo Clinical Research Support
Our pioneering clinical research approach to data collection and management revolutionizes healthcare and enhances patient outcomes through a multidisciplinary, innovative, and collaborative methodology that leverages cutting-edge technologies and upholds rigorous scientific practices.
Our clinical research approach is built on three pillars
Software
Innovative software for planning, collecting, and analyzing clinical and workflow data as well as improving operational study management and oversight.
Services
Comprehensive services portfolio, encompassing all stages of the clinical trial life cycle to provide high-quality results.
Global Capabilities Network
Innovative solutions with global reach to enhance clinical trials, including real-world data integration.
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
Reduce time to market
Improve data quality
Improve patient outcomes
ePRO & eCOA
Streamline data collection directly from patients and physicians to ensure highest data quality
Learn MoreRTSM
Automate randomization and investigational product supply management directly within the eCRF
Learn MoreCTMS
Oversee and manage your clinical trial effectively and efficiently with full integration across all Oomnia modules and customized dashboards
Learn MoreeConsent
Increase flexibility for patients while improving data quality and operational efficiencies with native EDC integration
Contact UsMedical Coding.
Assign medical codes directly in the eCRF during the data collection stage
Contact UsLab Management
Integrate central and local laboratory reference ranges, sample management, and data collection
Contact UsImaging
Collect image assessment results directly in the eCRF, integrated in the analytical data set
Contact UsQuery Management
Reduce the number of manual queries by over 60% through dynamic automated data cleaning
Contact UsMedical Device Data Integration
Integrate data feeds from wearables and centralized vendor databases directly into the eCRF
Contact UsServices
We provide comprehensive support and guidance throughout identification of requirements, protocol development, data management, statistical analysis, and final reporting 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
Contact UsData Management
Generate high-quality, reliable, and statistically sound data to support your clinical trial
Contact UsPharmacovigilance
Automate adverse event management to bolster patient safety surveillance in real-time
Contact UsBiostatistics
Unlock the true potential of your clinical trial data with accurate analyses and visualization
Contact UsMedical Writing
Let our highly qualified experts accelerate your trial to final submission-ready documents
Contact UsOomnia CRIS Customer Success
Advisory and Scoping
Leveraging insightful collaborative discussions, we tailor the system to amplify clinical trial design and data collection to align with your objectives
Contact UsTraining
We ensure your team is provided with relevant trainings and associated documentation throughout the trial
Contact UsGlobal Capabilities Network
Get enhanced and innovative global solutions through highly qualified, globally experienced, knowledgeable local experts within the AcrossGlobal Network.
Unlimited possibilities
Global reach
Unique solutions
Unique results
Rare Diseases
Expand your global reach to include underserved patients and regions through our alliance of CROs
Contact UsExperience 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 without downtime, even in an ongoing study.
Compatibility
The CDISC standard is integrated into every data field throughout the entire process, starting with the very first data entry.
Uniqueness
Unparalleled eCRF integration capabilities, including RTSM and centralized laboratory management, with real-time downloadable metrics and visualizations.
