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Chapman & Hall/CRC Biostatistics Series

About the Book Series

The primary objectives of the series are to provide useful reference books for researchers and scientists in academia, industry, and government, and also to offer textbooks for undergraduate and graduate courses in the areas of biostatistics and bioinformatics. The book series will provide comprehensive and unified presentations of statistical designs and analyses of important applications in biostatistics and bioinformatics, such as those in biological and biomedical research.

The scope of the series is wide, including applications of statistical methodology in biology, epidemiology, genetics, pharmaceutical science and clinical trials, public health, and medicine. The series is committed to providing easy to understand, state-of-the-art references and textbooks. In each volume, statistical concepts and methodologies will be illustrated through real world examples whenever possible.

Please contact us if you have an idea for a book for the series.

155 Series Titles


Essentials of a Successful Biostatistical Collaboration

Essentials of a Successful Biostatistical Collaboration

1st Edition

By Arul Earnest
June 30, 2020

The aim of this book is to equip biostatisticians and other quantitative scientists with the necessary skills, knowledge, and habits to collaborate effectively with clinicians in the healthcare field. The book provides valuable insight on where to look for information and material on sample size ...

Inference Principles for Biostatisticians

Inference Principles for Biostatisticians

1st Edition

By Ian C. Marschner
June 30, 2020

Designed for students training to become biostatisticians as well as practicing biostatisticians, Inference Principles for Biostatisticians presents the theoretical and conceptual foundations of biostatistics. It covers the theoretical underpinnings essential to understanding subsequent core ...

Interval-Censored Time-to-Event Data Methods and Applications

Interval-Censored Time-to-Event Data: Methods and Applications

1st Edition

Edited By Ding-Geng (Din) Chen, Jianguo Sun, Karl E. Peace
June 30, 2020

Interval-Censored Time-to-Event Data: Methods and Applications collects the most recent techniques, models, and computational tools for interval-censored time-to-event data. Top biostatisticians from academia, biopharmaceutical industries, and government agencies discuss how these advances are ...

Measures of Interobserver Agreement and Reliability

Measures of Interobserver Agreement and Reliability

2nd Edition

By Mohamed M. Shoukri
June 30, 2020

Measures of Interobserver Agreement and Reliability, Second Edition covers important issues related to the design and analysis of reliability and agreement studies. It examines factors affecting the degree of measurement errors in reliability generalization studies and characteristics influencing ...

Medical Product Safety Evaluation Biological Models and Statistical Methods

Medical Product Safety Evaluation: Biological Models and Statistical Methods

1st Edition

By Jie Chen, Joseph Heyse, Tze Leung Lai
June 30, 2020

Medical Product Safety Evaluation: Biological Models and Statistical Methods presents cutting-edge biological models and statistical methods that are tailored to specific objectives and data types for safety analysis and benefit-risk assessment. Some frequently encountered issues and challenges in ...

Noninferiority Testing in Clinical Trials Issues and Challenges

Noninferiority Testing in Clinical Trials: Issues and Challenges

1st Edition

By Tie-Hua Ng
June 30, 2020

Take Your NI Trial to the Next LevelReflecting the vast research on noninferiority (NI) designs from the past 15 years, Noninferiority Testing in Clinical Trials: Issues and Challenges explains how to choose the NI margin as a small fraction of the therapeutic effect of the active control in a ...

Quantitative Evaluation of Safety in Drug Development Design, Analysis and Reporting

Quantitative Evaluation of Safety in Drug Development: Design, Analysis and Reporting

1st Edition

Edited By Qi Jiang, H. Amy Xia
June 30, 2020

State-of-the-Art Methods for Drug Safety AssessmentResponding to the increased scrutiny of drug safety in recent years, Quantitative Evaluation of Safety in Drug Development: Design, Analysis and Reporting explains design, monitoring, analysis, and reporting issues for both clinical trials and ...

Quantitative Methods for HIV/AIDS Research

Quantitative Methods for HIV/AIDS Research

1st Edition

Edited By Cliburn Chan, Michael G. Hudgens, Shein-Chung Chow
June 30, 2020

Quantitative Methods in HIV/AIDS Research provides a comprehensive discussion of modern statistical approaches for the analysis of HIV/AIDS data. The first section focuses on statistical issues in clinical trials and epidemiology that are unique to or particularly challenging in HIV/AIDS research; ...

Randomized Clinical Trials of Nonpharmacological Treatments

Randomized Clinical Trials of Nonpharmacological Treatments

1st Edition

Edited By Isabelle Boutron, Philippe Ravaud, David Moher
June 30, 2020

Nonpharmacological treatments include a wide variety of treatments such as surgery, technical procedures, implantable and non-implantable devices, rehabilitation, psychotherapy, and behavioral interventions. Unlike pharmacological treatments, these have no specific requirements for approval. ...

Randomized Phase II Cancer Clinical Trials

Randomized Phase II Cancer Clinical Trials

1st Edition

By Sin-Ho Jung
June 30, 2020

In cancer research, a traditional phase II trial is designed as a single-arm trial that compares the experimental therapy to a historical control. This simple trial design has led to several adverse issues, including increased false positivity of phase II trial results and negative phase III trials...

Sample Size Calculations for Clustered and Longitudinal Outcomes in Clinical Research

Sample Size Calculations for Clustered and Longitudinal Outcomes in Clinical Research

1st Edition

By Chul Ahn, Moonseoung Heo, Song Zhang
June 30, 2020

Accurate sample size calculation ensures that clinical studies have adequate power to detect clinically meaningful effects. This results in the efficient use of resources and avoids exposing a disproportionate number of patients to experimental treatments caused by an overpowered study. Sample Size...

Statistical Analysis of Human Growth and Development

Statistical Analysis of Human Growth and Development

1st Edition

By Yin Bun Cheung
June 30, 2020

Statistical Analysis of Human Growth and Development is an accessible and practical guide to a wide range of basic and advanced statistical methods that are useful for studying human growth and development. Designed for nonstatisticians and statisticians new to the analysis of growth and ...

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