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Pharmaceutical Science Books

You are currently browsing 1–10 of 704 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. Nanoparticulate Vaccine Delivery Systems

    Edited by Martin J. D'Souza

    Recent years have seen the development of novel technologies that use nanoparticles and microparticles to deliver vaccines by the oral and transdermal routes of administration. These new technologies enable the formulation of vaccine particles that contain vaccine antigens, without loss of their...

    Published January 30th 2015 by Pan Stanford

  2. Noninvasive Molecular Markers in Gynecologic Cancers

    Edited by Debmalya Barh, Mehmet Gunduz

    Early detection is critical for any given cancer. With the advent of the latest omics technologies, molecular markers in combination with conventional diagnostic and screening methods are emerging as next-generation early diagnostic and prognostic strategies that can allow early-stage diagnosis,...

    Published January 21st 2015 by CRC Press

  3. Topical Antimicrobials Testing and Evaluation, Second Edition

    By Daryl S. Paulson

    A range of factors must be considered when developing a topical antimicrobial for use in a healthcare personnel handwash, surgical scrub, or preoperative skin preparation. Antimicrobial effectiveness, low skin irritation, ease of use, and pleasing aesthetics are all essential if the product is to...

    Published December 19th 2014 by CRC Press

  4. Statistical Methods in Drug Combination Studies

    Edited by Wei Zhao, Harry Yang

    Series: Chapman & Hall/CRC Biostatistics Series

    The growing interest in using combination drugs to treat various complex diseases has spawned the development of many novel statistical methodologies. The theoretical development, coupled with advances in statistical computing, makes it possible to apply these emerging statistical methods in in...

    Published December 18th 2014 by Chapman and Hall/CRC

  5. Creating Life from Life

    Biotechnology and Science Fiction

    Edited by Rosalyn W. Berne

    This book is a collection of essays by scientists, historians, philosophers of science, and students. The essays meld biotechnology into science fiction stories and thereby open a conversation about the morality of what we may be one day, and what it may mean to be human as our biotechnological...

    Published December 18th 2014 by Pan Stanford

  6. 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 14th 2014 by CRC Press

  7. Leadership and Management in Pharmacy Practice, Second Edition

    Edited by Andrew M. Peterson, William N. Kelly

    Series: Pharmacy Education Series

    Over the past years, the changing nature of pharmacy practice has caused many to realize that the practice must not only be managed, but also led. Leadership and Management in Pharmacy Practice discusses a variety of leadership and managerial issues facing pharmacists now and in the future. This...

    Published December 11th 2014 by CRC Press

  8. 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 8th 2014 by Chapman and Hall/CRC

  9. 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 7th 2014 by Chapman and Hall/CRC

  10. 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 November 30th 2014 by Chapman and Hall/CRC