New and Published Books
41-50 of 72 results in Chapman & Hall/CRC Biostatistics Series
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...
Published April 23rd 2009 by Chapman and Hall/CRC
Design and Analysis of Bioavailability and Bioequivalence Studies, Third Edition BABE-Solution bundle version
Containing four new chapters, along with several new and updated sections, this third edition reviews the latest progress of activities and results in bioavailability and bioequivalence on regulatory requirements, scientific and practical issues, and statistical methodology. It presents the current...
Published March 23rd 2009 by CRC Press
This book explains how the formulas and procedures for sample size calculations can be used in a variety of clinical research and development stages. It presents real-world examples from several therapeutic areas and explores emerging topics in pharmaceutical research and development. This edition...
Published March 23rd 2009 by Chapman and Hall/CRC
Focusing on the practical clinical and statistical issues that arise in pharmaceutical industry trials, this book summarizes the author’s experience in serving on many data monitoring committees (DMCs) and in heading up a contract research organization that provided statistical support to nearly...
Published March 13th 2009 by Chapman and Hall/CRC
Using WinBUGS to implement Bayesian inferences of estimation and testing hypotheses, Bayesian Methods for Measures of Agreement presents useful methods for the design and analysis of agreement studies. It focuses on agreement among the various players in the diagnostic process. The author employs...
Published January 12th 2009 by Chapman and Hall/CRC
Strategies and Statistical Methods
Examines Critical Decisions for Transitioning Lab Science to a Clinical SettingThe development of therapeutic pharmaceutical compounds is becoming more expensive, and the success rates for getting such treatments approved for marketing and to the patients is decreasing. As a result, translational...
Published December 17th 2008 by Chapman and Hall/CRC
Preeminent Experts Update a Well-Respected Book Taking into account the regulatory and scientific developments that have occurred since the second edition, Design and Analysis of Bioavailability and Bioequivalence Studies, Third Edition provides a complete presentation of the latest progress of...
Published October 15th 2008 by Chapman and Hall/CRC
Experimental Design and Statistical Analysis
Providing an interface between dry-bench bioinformaticians and wet-lab biologists, DNA Methylation Microarrays: Experimental Design and Statistical Analysis presents the statistical methods and tools to analyze high-throughput epigenomic data, in particular, DNA methylation microarray data. Since...
Published April 24th 2008 by Chapman and Hall/CRC
Continuing advances in biomedical research and statistical methods call for a constant stream of updated, cohesive accounts of new developments so that the methodologies can be properly implemented in the biomedical field. Responding to this need, Computational Methods in Biomedical Research...
Published December 12th 2007 by Chapman and Hall/CRC
Focusing on an integral part of pharmaceutical development, Sample Size Calculations in Clinical Research, Second Edition presents statistical procedures for performing sample size calculations during various phases of clinical research and development. It provides sample size formulas and...
Published August 22nd 2007 by Chapman and Hall/CRC
Adaptive Design Theory and Implementation Using SAS and R, Second Edition
To Be Published December 4th 2014
Noninferiority Testing in Clinical Trials: Issues and Challenges
To Be Published December 5th 2014
Quantitative Evaluation of Safety in Drug Development: Design, Analysis and Reporting
To Be Published December 9th 2014
Inference Principles for Biostatisticians
To Be Published December 10th 2014
Sample Size Calculations for Clustered and Longitudinal Outcomes in Clinical Research
To Be Published December 30th 2014
Statistical Methods in Drug Combination Studies
To Be Published January 5th 2015
Design and Analysis of Clinical Trials for Predictive Medicine
To Be Published March 24th 2015
Adaptive Designs for Sequential Treatment Allocation
To Be Published April 15th 2015
Statistical Design and Analysis of Clinical Trials: Principles and Methods
To Be Published May 15th 2015
Clinical Trial Simulations
To Be Published May 25th 2015