Basic

JMP® Clinical: Centralized Statistical Monitoring of Clinical Trials

Application Area:
Life Sciences

This session is for JMP Clinical users interested in moving away from 100% source data
verification and costly on-site visits to manage clinical trial operational quality in line with recent regulatory guidance.  See how to use statistical sampling and calculation of risk scores on key performance metrics to help investigators uncover data quality issues, identify fraudulent activity, and determine how clinical trial sites can benefit from monitoring or corrective action. 

This webinar covers: Risk-Based Monitoring; digit preferences; unusual subject similarities; duplicated or constant findings; and unexpected enrollment or visit patterns.

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