is_orivisit

internal

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
simulations during which patients are redistributed between sites. Site-specific
distributions of event reporting rates are generated that are used to assign
probabilities to the observed reporting rates.
(Koneswarakantha 2024 <doi:10.1007/s43441-024-00631-8>).

Bjoern Koneswarakantha

simaerep

Detect Clinical Trial Sites Over- or Under-Reporting Clinical
Events

F. Hoffmann-La Roche Ltd 

is_orivisit function

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

Arguments

is orivisit class — is_orivisit

<dl>

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

</dl>

is_orivisit: is orivisit class

Description

Usage

Value

Arguments