Manage all your clinical trial data from a single source
Why Choose CDR?
Don’t let valuable data sit on the sidelines. Transform collected data into valuable information and insights-"faster"-by bringing your data into a centralized data management hub.
Benefits
Aggregate and standardize source- and type- agnostic data to support multi-modal data review and analysis.
Conduct data reviews and run analytics anytime within a self-service environment.
View data in near-real time with a custom dashboards and visualizations.
Gain a holistic view of clinical trials and patient outcomes.
Perform quality reviews sooner with automated data standardization.
Improve trial efficiency for revenue and quality gains.
Key features
High data variety and volume
Store high volumes of data across all formats, sizes, and types.
Data slice and dice
Create data snapshots and data marts to address access needs across departments and stakeholders.
High manageability
Built-in version and change controls, snapshot management, organization structure management, data model management, backup and archive management, role-based access management, and data provisioning management.
Advanced analytics
Preconfigured out-of-the-box reports and visualizations support a wide range of descriptive and data-driven analytics.
Controlled data view
Viewing data in blinded, unblinded or de-identified modes based on assigned roles and access privileges.
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.
Executive Management
Utilize CDR to streamline clinical trial processes, enhancing data collection and accelerating drug development.
Leverage comprehensive data to assess pharmacoeconomic performance and demonstrate value to payers.
Medical Monitoring
Integrate and aggregate clinical data into a central hub, ready for analysis, ensuring comprehensive and accurate information.
Review data in real time to assess safety risks as they happen, allowing for immediate action and improved patient safety.
Clinical Data Management
Automate data processing steps and streamline data discrepancy detection with CDR for early issue resolution.
Aggregate and standardize data from multiple sources and types to support multi-modal data review and analysis.
Biostatistics and Programming
Seamlessly integrate data from various sources and automate end-to-end data pipelines with CDR.
Transform raw data into SDTM, ADaM, and other regulatory formats using CDR for accurate and compliant reporting.
R&D and IT
Eliminate data silos by using CDR to allow seamless data integration across various platforms, improving efficiency and collaboration.
Ensure data integrity and compliance with validation, metadata management, and data lineage tracking. Support for SDTM, ODM, CDASH, and ADAM standards unifies and streamlines data management.
About MaxisIT
MaxisIT’s purpose-fit and intelligent clinical data analytics platform helps improve clinical trial performance, mitigate risk, and optimize clinical outcomes. We provide a centralized and reliable source of truth for diverse data types from various sources, giving life sciences companies real-time insight to shorten cycle time and increase return on investment. Incorporating an end-to-end clinical data pipeline from intake to visualization, MaxisIT's solutions are powered by AI/ML and metadata-centric approaches. Our impressive portfolio of over 3,300 clinical trials and an unparalleled 100% customer retention rate affirm the quality and reliability of our services.
“Implementation of MaxisIT’s clinical data repository enabled us easier, and faster access to our outsourced trials’ data in the most user-friendly manner, which improved our ability to respond to data quality issues, and conduct clinical data review in timely manner.”
Executive Director and Senior Physician Project Leader Neurosciences
Focused Business Subsidiary of one of the top 10 Pharmaceutical Companies
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