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

    • ¥11,800
    • ¥11,800

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
April 23
LANGUAGE
EN
English
LENGTH
616
Pages
PUBLISHER
CRC Press
SELLER
Taylor & Francis Group
SIZE
10.8
MB
Applied Meta-Analysis with R and Stata Applied Meta-Analysis with R and Stata
2021
Statistical Issues in Drug Research and Development Statistical Issues in Drug Research and Development
2017
Clinical Trial Data Analysis Using R and SAS Clinical Trial Data Analysis Using R and SAS
2017
Advanced Statistical Analytics for Health Data Science with SAS and R Advanced Statistical Analytics for Health Data Science with SAS and R
2025
R for Health Technology Assessment R for Health Technology Assessment
2025
Generalized Linear Models Generalized Linear Models
2000
Statistics In the Pharmaceutical Industry Statistics In the Pharmaceutical Industry
2019
Design and Analysis of Animal Studies in Pharmaceutical Development Design and Analysis of Animal Studies in Pharmaceutical Development
1998
Applied Statistical Designs for the Researcher Applied Statistical Designs for the Researcher
2003