Create a compliant clinical IT foundation with automated metadata management
Higher data accuracy rate in statistical analyses
Reduction of programming time
Reduction in errors through rigorous quality control measures
Higher data accuracy rate in statistical analyses
Reduction of programming time
Reduction in errors through rigorous quality control measures
Higher data accuracy rate in statistical analyses
Reduction of programming time
Reduction in errors through rigorous quality control measures
Maximize your resources and your metadata
Are manual programming and data reviews holding back your clinical IT initiatives?
Disconnected systems and outdated technology can’t handle today’s data-intensive clinical trials. A scalable clinical data analytics platform with metadata repository gives you the flexibility to build advanced data management and analytics systems without custom programming and with limitless scalability.
MaxisIT operates on a philosophy of data integration, automation, and standardization.
Provides structure and flexibility with no data formatting required, ensuring ease of use and efficiency.
Your data are not held in silos, allowing for seamless data integration across various platforms.
Data validation, metadata management, and data lineage tracking ensure data integrity and regulatory compliance.
Role-based access keeps data secure. All products are 21 CFR Part 11 compliant for added security.
Out-of-the-box solution and low-code/no-code environments for quick and hassle-free setup.
Supports SDTM, ODM, CDASH, and ADAM data standards for streamlined and compliant data management.
MaxisIT Data Management Workbench
See how MaxisIT supports R&D IT
MaxisIT helps pharmaceutical and biopharmaceutical companies of all sizes plan and execute effective clinical trials. Our source-agnostic integrated clinical data analytics platform unifies data across clinical systems and CROs to enable real-time monitoring and on-time insights.
