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Pharmaceutical Science Books

You are currently browsing 1–10 of 702 new and published books in the subject of Pharmaceutical Science — sorted by publish date from newer books to older books.

For books that are not yet published; please browse forthcoming books.

New and Published Books

  1. Quantitative Evaluation of Safety in Drug Development

    Design, Analysis and Reporting

    Edited by Qi Jiang, H. Amy Xia

    Series: Chapman & Hall/CRC Biostatistics Series

    State-of-the-Art Methods for Drug Safety Assessment Responding 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...

    Published December 18th 2014 by Chapman and Hall/CRC

  2. Pharmaceutical and Medical Applications of Near-Infrared Spectroscopy, Second Edition

    By Emil W. Ciurczak, Benoit Igne

    Series: Practical Spectroscopy

    Since the completion of the first edition of this book, major developments have occurred in the pharmaceutical industry that have shaped the field of near-infrared (NIR) spectroscopy. A new initiative from the U.S. Food and Drug Administration (FDA) to modernize regulations of pharmaceutical...

    Published December 17th 2014 by CRC Press

  3. Sample Size Calculations for Clustered and Longitudinal Outcomes in Clinical Research

    By Chul Ahn, Moonseoung Heo, Song Zhang

    Series: Chapman & Hall/CRC Biostatistics Series

    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...

    Published December 17th 2014 by Chapman and Hall/CRC

  4. Mechanobiology of the Endothelium

    Edited by Helim Aranda-Espinoza

    The endothelium is an excellent example of where biology meets physics and engineering. It must convert mechanical forces into chemical signals to maintain homeostasis. It also controls the immune response, drug delivery through the vasculature, and cancer metastasis. Basic understanding of these...

    Published December 15th 2014 by CRC Press

  5. Noninferiority Testing in Clinical Trials

    Issues and Challenges

    By Tie-Hua Ng

    Series: Chapman & Hall/CRC Biostatistics Series

    Take Your NI Trial to the Next Level Reflecting 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...

    Published December 1st 2014 by Chapman and Hall/CRC

  6. Adaptive Design Theory and Implementation Using SAS and R, Second Edition

    By Mark Chang

    Series: Chapman & Hall/CRC Biostatistics Series

    Get Up to Speed on Many Types of Adaptive Designs Since the publication of the first edition, there have been remarkable advances in the methodology and application of adaptive trials. Incorporating many of these new developments, Adaptive Design Theory and Implementation Using SAS and R, Second...

    Published December 1st 2014 by Chapman and Hall/CRC

  7. Pharmacology and Aphasia

    Edited by Marcelo L. Berthier, Guadalupe Davila

    This book provides clinicians and researchers with the current state-of-the-art on the pharmacological treatment of aphasia. The focus is on the role of different pharmacological agents to improve aphasia associated with stroke and to attenuate language dissolution in degenerative conditions like...

    Published November 28th 2014 by Routledge

  8. Clinical Trial Biostatistics and Biopharmaceutical Applications

    Edited by Walter R. Young, Ding-Geng (Din) Chen

    Since 1945, "The Annual Deming Conference on Applied Statistics" has been an important event in the statistics profession. In Clinical Trial Biostatistics and Biopharmaceutical Applications, prominent speakers from past Deming conferences present novel biostatistical methodologies in clinical...

    Published November 20th 2014 by Chapman and Hall/CRC

  9. Handbook of Bioequivalence Testing, Second Edition

    By Sarfaraz K. Niazi

    Series: Drugs and the Pharmaceutical Sciences

    As the generic pharmaceutical industry continues to grow and thrive, so does the need to conduct adequate, efficient bioequivalence studies. In recent years, there have been significant changes to the statistical models for evaluating bioequivalence. In addition, advances in the analytical...

    Published October 29th 2014 by CRC Press

  10. Re-inventing Drug Development

    Edited by Jeffrey S. Handen

    The biopharmaceutical industry has entered an era of unprecedented change and challenge, characterized by increasing pricing pressures, rising rates of attrition in the product development lifecycle, and decreasing scientific innovation. The most successful products are losing patent protection,...

    Published October 28th 2014 by CRC Press