Software that complies with regulatory criteria is utilized in clinical trial monitoring and is called Risk Based Monitoring software.
Using a variety of tools, platforms, and dashboards, Risk Based Monitoring (RBM), a clinical trial monitoring technique that satisfies regulatory requirements, looks for signals that could point to problems with trial conduct, safety, compliance, and data integrity.
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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