TRIAL DATA AS A SINGLE SOURCE-OF-TRUTH
MaxisIT’s Clinical Trials Oversight System maintains a single-source-of-truth data hub supporting the integration and aggregation of all clinical trial data from various eClinical systems & partner CRO's systems and intelligently analyzes it to gather insights.
Make Informed Decisions
Sponsors can make informed decisions as they review clinical data quality, monitor trial performance in real-time, assess safety and risks, ensuring regulatory compliance and keeping the studies on time and within budget.
How Does It Work?
Single-source-of -truth – Real-time, automated aggregation across various siloed EDCs, LABs, IRTs, ePROs, CTMSs and other eClinical systems into a single data hub
Continuous Oversight Real-time view of trial status. Patient Data and Clinical Operations’ oversight, performance KPIs, Data Quality Management and risk management.
Insights - Achieve patient centricity and gain efficiency in clinical trials, with proactive insights.
Risk mitigation – Red-flags errors in real-time to eliminate risk
Analytical Dashboards Intuitive, role-based dashboards.
Analysis – Robust, AI-powered analysis of end-to-end clinical trial data
In-time Action - Actionable insights for timely intervention. Decisions are made possible with access to real-time, accurate information
Compliance - Keep the studies compliant, on time and within budget.