simaerep

cranv1.0.0

Detect Clinical Trial Sites Over- or Under-Reporting Clinical Events. Monitoring reporting rates of subject-level clinical events (e.g. adverse events, protocol deviations) reported by clinical trial sites is an important aspect of risk-based quality monitoring strategy. Sites that are under-reporting or over-reporting events can be detected using bootstrap simulation

License MIT + file LICENSE0 versions1 maintainers16 deps51 weekly dl
openpharma/simaerep/
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First published · 2025-10-28 11:52:56

Last updated · 2025-10-28T10:40:02+00:00