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^\.git | ||
^cran-comments\.md$ | ||
^data-raw$ | ||
^CRAN-SUBMISSION$ |
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Package: simaerep | ||
Title: Simulate Adverse Event Reporting in Clinical Trials with the Goal of Detecting under-Reporting Sites | ||
Title: Find Clinical Trial Sites Under-Reporting Adverse Events | ||
Version: 0.4.2 | ||
Authors@R: | ||
Authors@R: c( | ||
person(given = "Bjoern", | ||
family = "Koneswarakantha", | ||
role = c("aut", "cre"), | ||
role = c("aut", "cre", "cph"), | ||
email = "[email protected]", | ||
comment = c(ORCID = "0000-0003-4585-7799")) | ||
Description: This can detect clinical trial sites that are under-reporting adverse events (AE). | ||
Bootstrap-based simulations are used to simulate AE reporting and to assign an AE | ||
under-reporting probability to each site in a clinical trial (Koneswarakantha 2021 | ||
<doi:10.1007/s40264-020-01011-5>). | ||
comment = c(ORCID = "0000-0003-4585-7799")), | ||
person("F. Hoffmann-La Roche Ltd", | ||
role = c("cph")) | ||
) | ||
Description: 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>). | ||
URL: https://openpharma.github.io/simaerep/, https://github.com/openpharma/simaerep | ||
License: MIT + file LICENSE | ||
Encoding: UTF-8 | ||
|
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#' @export | ||
#' @importFrom magrittr %>% | ||
#' @usage lhs \%>\% rhs | ||
#' @return returns output of rhs function | ||
NULL |
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@@ -95,6 +95,3 @@ reference: | |
- plot_sim_examples | ||
- plot_sim_example | ||
- plot_dots | ||
- title: internal | ||
contents: | ||
- lint_package |
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