is_simaerep

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>).

Bjoern Koneswarakantha

simaerep

Find Clinical Trial Sites Under-Reporting Adverse Events

F. Hoffmann-La Roche Ltd 

is_simaerep function

<dl><dt>x</dt>
<dd>object</dd></dl>

Arguments

is simaerep class — is_simaerep

<dl>

<dt>x</dt>
<dd>object</dd>

</dl>

is_simaerep: is simaerep class

Description

Usage

Value

Arguments