Risk Based Monitoring means that the volume and frequency of monitoring is minimized.
Clinical teams have access to a single platform through Risk Based Monitoring software that converts various study data streams into useful insights. As a result, monitoring efforts are more targeted and data-driven, which enables sponsor supervision and raises the standard and compliance of a clinical study or program.
As data are only checked at high risk sites based on triggered events or specific pre-defined key events in the research, Risk Based Monitoring means that the volume and frequency of monitoring is minimized. By identifying, evaluating, monitoring, and limiting risks, the quality of the trial data can be increased.
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