simaerep: Find Clinical Trial Sites Under-Reporting Adverse Events

Monitoring of Adverse Event (AE) reporting in clinical trials is important for patient safety. Sites that are under-reporting AEs can be detected using Bootstrap-based simulations that simulate overall AE reporting. Based on the simulation an AE under-reporting probability is assigned to each site in a given trial (Koneswarakantha 2021 <doi:10.1007/s40264-020-01011-5>).

Version: 0.5.0
Depends: R (≥ 4.0), ggplot2
Imports: dplyr (≥ 1.0.0), tidyr (≥ 1.1.0), magrittr, purrr, rlang, stringr, forcats, cowplot, RColorBrewer, furrr (≥ 0.2.1), progressr, knitr, tibble
Suggests: testthat, devtools, pkgdown, spelling, haven, vdiffr, lintr
Published: 2024-04-03
DOI: 10.32614/CRAN.package.simaerep
Author: Bjoern Koneswarakantha ORCID iD [aut, cre, cph], F. Hoffmann-La Roche Ltd [cph]
Maintainer: Bjoern Koneswarakantha <bjoern.koneswarakantha at>
License: MIT + file LICENSE
NeedsCompilation: no
Language: en-US
Materials: README NEWS
CRAN checks: simaerep results


Reference manual: simaerep.pdf


Package source: simaerep_0.5.0.tar.gz
Windows binaries: r-devel:, r-release:, r-oldrel:
macOS binaries: r-release (arm64): simaerep_0.5.0.tgz, r-oldrel (arm64): simaerep_0.5.0.tgz, r-release (x86_64): simaerep_0.5.0.tgz, r-oldrel (x86_64): simaerep_0.5.0.tgz
Old sources: simaerep archive


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