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?

Aggregate

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.

Inform

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.

Analyze

Analysis – Robust, AI-powered analysis of end-to-end clinical trial data

Support

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.

MaxisIT's CTOS

Trusted globally

Currently being used in over 2000 clinical trials and counting.

Secures access to Data

Role-based access to data in the cloud.

Saves Time and Cost

Pay-as-you-go subscriptions. Minimum run cost.

KEEP YOUR CLINICAL TRIALS ON-TIME AND WITHIN BUDGET

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