Manage all your clinical trial data from a single source
Unlock more power from your clinical trial data
Integrate and standardize clinical and healthcare data into formats you can use to deliver your products to more patients.
Bring all your data together for robust insights that make an impact
Standardize structured and unstructured data to deliver robust insights for risk-based monitoring, data management, and analytics.
A comprehensive platform for managing data, metadata, reporting, and analytics for sponsors, sites, and CROs, consolidating all your clinical data needs.
Conduct data reviews and analytics anytime within a user-friendly, self-service environment, empowering your team to analyze data independently.
View data in near-real time with custom dashboards and visualizations, gaining immediate insights for quicker, informed decision-making.
Perform quality reviews sooner with automated data standardization, ensuring consistency and accuracy across all datasets.
Improve trial efficiency, leading to significant revenue and quality gains by optimizing processes and achieving faster, more reliable results.
Data integration and standardization are two of the top challenges facing data management. CDR brings together all your data into one central location for richer analyses and improved data quality and integrity.
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.