Design and Analysis of Clinical Trials with Time-to-Event Endpoints e-bog
509,93 DKK
(inkl. moms 637,41 DKK)
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 "e;noninformativeness"e; of the censoring mechanisms relative to the event. Design and Analysis of Clinical Trials with Time-to-Event Endpoints provides a thorough presentation o
E-bog
509,93 DKK
Forlag
Chapman and Hall/CRC
Udgivet
23 april 2009
Længde
616 sider
Genrer
MBGR1
Sprog
English
Format
pdf
Beskyttelse
LCP
ISBN
9781420066401
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 "e;noninformativeness"e; of the censoring mechanisms relative to the event. Design and Analysis of Clinical Trials with Time-to-Event Endpoints provides a thorough presentation o