Design and Analysis of Clinical Trials with Time-to-Event Endpoints Design and Analysis of Clinical Trials with Time-to-Event Endpoints
Chapman & Hall/CRC Biostatistics Series

Design and Analysis of Clinical Trials with Time-to-Event Endpoints

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Publisher Description

Using time-to-event analysis methodology requires careful definition of the event, censored observation, provision of adequate follow-up, number of events, and independence or "noninformativeness" of the censoring mechanisms relative to the event. Design and Analysis of Clinical Trials with Time-to-Event Endpoints provides a thorough presentation o

GENRE
Science & Nature
RELEASED
2009
23 April
LANGUAGE
EN
English
LENGTH
616
Pages
PUBLISHER
CRC Press
SIZE
10.8
MB
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