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Overview
*Short Courses require an additional registration fee. You do not need to be registered for the forum to attend*
This Short Course will be offering in a virtual format only
This (mainly) formula-free half-day course will introduce a systematic approach for evaluating and assessing adverse events and other safety information, guided by medical judgment, which enables investigators to develop clinical as well as statistical understanding of the safety profile.
Topics to be covered include:
- Denominators and numerators, variability, confidence intervals, p-values, and significance
- Absolute risk, risk ratios, odds ratios, and hazard ratios – when, why, and what to look for
- Safety estimands
- Common abuses of statistics in PV
- Quantitative frameworks for measuring evidence of association
- A multidisciplinary approach that incorporates quantitative methods with clinical judgment
- Scientific evaluation of accumulating program-level safety information throughout drug development
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