New and Published Books
21-30 of 59 results in Chapman & Hall/CRC Biostatistics Series
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Clinical Trial Data Analysis Using R
Series: Chapman & Hall/CRC Biostatistics Series
Too often in biostatistical research and clinical trials, a knowledge gap exists between developed statistical methods and the applications of these methods. Filling this gap, Clinical Trial Data Analysis Using R provides a thorough presentation of biostatistical analyses of clinical trial data and...
Published December 13th 2010 by CRC Press
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Adaptive Design Methods in Clinical Trials
Series: Chapman & Hall/CRC Biostatistics Series
Although adaptive design methods are flexible and useful in clinical research, little or no regulatory guidelines are available. One of the first books on the topic, Adaptive Design Methods in Clinical Trials presents the principles and methodologies in adaptive design and analysis that pertain to...
Published December 11th 2010 by Chapman and Hall/CRC
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Monte Carlo Simulation for the Pharmaceutical Industry
Concepts, Algorithms, and Case Studies
Series: Chapman & Hall/CRC Biostatistics Series
Helping you become a creative, logical thinker and skillful "simulator," Monte Carlo Simulation for the Pharmaceutical Industry: Concepts, Algorithms, and Case Studies provides broad coverage of the entire drug development process, from drug discovery to preclinical and clinical trial aspects to...
Published September 28th 2010 by CRC Press
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Bayesian Modeling in Bioinformatics
Series: Chapman & Hall/CRC Biostatistics Series
Bayesian Modeling in Bioinformatics discusses the development and application of Bayesian statistical methods for the analysis of high-throughput bioinformatics data arising from problems in molecular and structural biology and disease-related medical research, such as cancer. It presents a broad...
Published September 2nd 2010 by Chapman and Hall/CRC
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Frailty Models in Survival Analysis
Series: Chapman & Hall/CRC Biostatistics Series
The concept of frailty offers a convenient way to introduce unobserved heterogeneity and associations into models for survival data. In its simplest form, frailty is an unobserved random proportionality factor that modifies the hazard function of an individual or a group of related individuals....
Published July 25th 2010 by Chapman and Hall/CRC
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Clinical Trial Methodology
Series: Chapman & Hall/CRC Biostatistics Series
Now viewed as its own scientific discipline, clinical trial methodology encompasses the methods required for the protection of participants in a clinical trial and the methods necessary to provide a valid inference about the objective of the trial. Drawing from the authors’ courses on the subject...
Published July 19th 2010 by Chapman and Hall/CRC
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Bayesian Adaptive Methods for Clinical Trials
Series: Chapman & Hall/CRC Biostatistics Series
Already popular in the analysis of medical device trials, adaptive Bayesian designs are increasingly being used in drug development for a wide variety of diseases and conditions, from Alzheimer’s disease and multiple sclerosis to obesity, diabetes, hepatitis C, and HIV. Written by leading pioneers...
Published July 18th 2010 by CRC Press
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Multiple Testing Problems in Pharmaceutical Statistics
Series: Chapman & Hall/CRC Biostatistics Series
Useful Statistical Approaches for Addressing Multiplicity IssuesIncludes practical examples from recent trials Bringing together leading statisticians, scientists, and clinicians from the pharmaceutical industry, academia, and regulatory agencies, Multiple Testing Problems in Pharmaceutical...
Published December 7th 2009 by Chapman and Hall/CRC
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Bayesian Missing Data Problems
EM, Data Augmentation and Noniterative Computation
Series: Chapman & Hall/CRC Biostatistics Series
Bayesian Missing Data Problems: EM, Data Augmentation and Noniterative Computation presents solutions to missing data problems through explicit or noniterative sampling calculation of Bayesian posteriors. The methods are based on the inverse Bayes formulae discovered by one of the author in 1995....
Published August 25th 2009 by Chapman and Hall/CRC
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Design and Analysis of Clinical Trials with Time-to-Event Endpoints
Series: 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 22nd 2009 by Chapman and Hall/CRC
Forthcoming Books
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Applied Meta-Analysis with R
To Be Published May 22nd 2013 -
Survival Analysis in Medicine and Genetics
To Be Published June 17th 2013 -
Optimal Design for Nonlinear Response Models
To Be Published July 22nd 2013 -
Biosimilars: Design and Analysis of Follow-on Biologics
To Be Published August 1st 2013 -
Bayesian Methods in Epidemiology
To Be Published August 22nd 2013 -
Theory of Drug Development
To Be Published September 23rd 2013 -
Statistical Analysis of Human Growth and Development
To Be Published November 7th 2013 -
Benefit-Risk Assessment in Pharmaceutical Research and Development
To Be Published November 25th 2013 -
Patient-Reported Outcomes: Measurement, Implementation and Interpretation
To Be Published January 14th 2014 -
Equivalency and Noninferiority Testing in Clinical Trials: Issues and Challenges
To Be Published February 24th 2014