Robust clinical data management and analytics from ingestion to reporting
Why Choose CTRenaissance®?
Validated, compliant, and powerfully automated, our integrated clinical data analytics platform provides configurable end-to-end data pipelines for seamless clinical research.
Benefits
Accelerate study cycle times by avoiding manual reconciliation and data review.
Enable risk-based quality management (RBQM) approaches.
Enhance operational efficiency and collaboration with AI-powered automation.
Perform real-time risk assessment and mitigation.
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CTRenaissance® Clinical Data Analytics Platform
Key features
Build Your Data Pipeline
Build an end-to-end data pipeline in no time with the help of automation. Includes source- and format-agnostic integrations across 40+ clinical operations and patient data sources.
Leverage Artificial Intelligence and Machine Learning (AI/ML)
All MaxisIT solutions are powered by advanced AI/ML and metadata-centric approaches for more robust insights, faster.
Streamline Clinical Data Management
Remove data management bottlenecks with a platform that brings virtually all data sources together in a flash. Automation takes care of the data ingestion, cleaning, and standardization, saving weeks to months off the process.
Drive Intelligent Decision-Making
Custom dashboards and visualizations show the right information, to the right stakeholders, in near-real time. Laser focus on patient safety, clinical efficacy, site performance, and more.
Simplify Statistical Programming
Move from reactive to proactive with a system that brings in data from all sources into a centralized data repository. Reach from data ingestion to insights in record time with the help of AI-powered tools.
Vendor-agnostic data storage, support for most programming languages, and a collaborative environment give your programmers and statisticians the tools to create expert analyses and submission-ready reports. Full audit trails, version control, and traceability assure compliance.
Explore CTRenaissance® Modules
Clinical Trials Oversight System (CTOS)
CTOS is a flexible platform designed to help complex clinical trials - traditional site-based, decentralized, hybrid, or 100% virtual.
Using advanced automation, CTOS brings greater visibility to your trial data at both the study and portfolio levels.
Clinical Data Repository (CDR)
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.
Data Management Workbench (DMW)
Data management workbench is your centralized command center for end-to-end clinical data management and data quality management.
Move from data capture to compliant reporting weeks faster with a purpose-built data management hub.
Risk-Based Quality Management (RBQM)
From collaborative workflows to detailed reporting, MaxisIT’s RBQM solution suits all study types and designs.
Our dedicated solution works with our entire product suite to de-risk trial operations and management.
Statistical Computing Environment (SCE)
Reduce risk of missteps by bringing data into the centralized, cloud-based SCE.
With advanced data analytics, real-time collaboration, and support for most programming languages, SCE brings power and precision to your clinical research.
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.
“Right combination of technology, process, and qualified people delivered via MaxisIT partnership enabled us to achieve above 50% reduction in protocol cycle time across the portfolio of trials, and also establish clear visibility across the trial performance.”
Head, Clinical Data Management
A multi-billion Medical Device company
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