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Robust clinical data management and analytics from ingestion to reporting
Clinical Trials Oversight System
Clinical Trials Oversight System
Gain full visibility across your trial portfolio—in real time
Data Management Workbench
Data Management Workbench
Seamless clinical data management is possible with the right integrations
Statistical Computing Environment
Statistical Computing Environment
Accelerate your clinical research with powerful statistical programming
Clinical Data Repository
Clinical Data Repository
Manage all your clinical trial data from a single source
Risk-based Quality Management
Risk-based Quality Management
Monitor and mitigate risks with an integrated RBQM solution
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Smart Optimizer
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Biostatistics and Programming
Quality data for analytics and reporting
Medical Monitoring
Medical Monitoring
Safe clinical trials start with unified patient safety data
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Executive Management
Full data access to optimise clinical trial risk management and drive brand success
Research and Development, Information Technology
Research and Development, Information Technology
Create a compliant clinical IT foundation with automated metadata management
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ARTICLE

Value-Based Data: Real-World Comparison

Exploring the integration of real-world data (RWD) in clinical trials: Can sponsors use it to enhance safety and efficacy assessments? Discover how external control arms are reshaping traditional approaches, potentially replacing standard control groups.
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What is an External Control Arm?
How to Use Real-World Data to Develop External Control Arms for Clinical Trials?
What are the BENEFITS of an External Control Arm?

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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.