RiskMonitor enables life sciences companies to target and prioritize resources around identifiable risks relating to the safety of subjects and quality and integrity of clinical trial data. It allows organization to limit the amount of Source Data Verification (SDV) at the study, site and/or subject level.  Organization equipped with RiskMonitor will be able to perform targeted monitoring which is a way of reducing SDV to a targeted number of data points.  It also allows organization to do trigger based monitoring wherein a trigger is defined for the detection of an issue or amount of data outstanding that requires SDV.

• Reduces the source data verification by targeted monitoring and trigger based monitoring
• Reduces the overall onsite monitoring
• Enables remote monitoring
• It minimizes data queries
• It increases productivity