Pharmaceutical Science Books

New and Published Books

1. Applied Meta-Analysis with R

   By Ding-Geng (Din) Chen, Karl E. Peace

   Series: Chapman & Hall/CRC Biostatistics Series

   In biostatistical research and courses, practitioners and students often lack a thorough understanding of how to apply statistical methods to synthesize biomedical and clinical trial data. Filling this knowledge gap, Applied Meta-Analysis with R shows how to implement statistical meta-analysis...

   Published May 22nd 2013 by Chapman and Hall/CRC
2. Randomized Phase II Cancer Clinical Trials

   By Sin-Ho Jung

   Series: Chapman & Hall/CRC Biostatistics Series

   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...

   Published May 1st 2013 by Chapman and Hall/CRC
3. Toxicologic Pathology

   Nonclinical Safety Assessment

   Edited by Pritam Sahota, James A. Popp, Jerry F. Hardisty, Chirukandath Gopinath

   As drug development shifts over time to address unmet medical needs and more targeted therapies are developed, previously unseen pharmacological or off-target effects may occur in treatment. Designed to provide practical information for the bench toxicologic pathologist working in pharmaceutical...

   Published April 8th 2013 by CRC Press
4. Applying Genomic and Proteomic Microarray Technology in Drug Discovery, Second Edition

   By Robert S. Matson

   Microarrays play an increasingly significant role in drug discovery. The commercial landscape has changed dramatically over the past few years and researchers have made great advancements with regard to construction and use. Now in its second edition, Applying Genomic and Proteomic Microarray...

   Published March 12th 2013 by CRC Press
5. A Practical Guide to Human Research and Clinical Trials

   By M. U. R. Naidu, P. Usha Rani

   Regulatory bodies such as the European Medicine Agency have done tremendous work in collaboration with experts from the field to develop Good Clinical Practices that apply not only in Europe but also in emerging countries. Designed to be a teaching aid and reference guide, A Practical Guide to...

   Published January 28th 2013 by CRC Press
6. Pharmaceutical Dosage Forms - Parenteral Medications

   Regulations, Validation and the Future, 3rd Edition

   Edited by Sandeep Nema, John D. Ludwig

   This three-volume set of Pharmaceutical Dosage Forms: Parenteral Medications is an authoritative, comprehensive reference work on the formulation and manufacture of parenteral dosage forms, effectively balancing theoretical considerations with the practical aspects of their development. As such, it...

   Published December 26th 2012 by CRC Press
7. Encyclopedia of Biopharmaceutical Statistics, Third Edition

   Edited by Shein-Chung Chow

   In recent years, there has been an explosive growth of biopharmaceutical and clinical research, including the development of new medicines for treating severe or life-threatening diseases. Biopharmaceutical statistics plays an extremely important role in ensuring not only the efficacy and safety of...

   Published December 26th 2012 by CRC Press
8. Pharmaceutical Dosage Forms - Parenteral Medications

   Facility Design, Sterilization and Processing, 3rd Edition

   Edited by Sandeep Nema, John D. Ludwig

   This three-volume set of Pharmaceutical Dosage Forms: Parenteral Medications is an authoritative, comprehensive reference work on the formulation and manufacture of parenteral dosage forms, effectively balancing theoretical considerations with the practical aspects of their development. As such, it...

   Published December 14th 2012 by CRC Press
9. Pharmaceutical Dosage Forms - Parenteral Medications

   Formulation and Packaging, 3rd Edition

   Edited by Sandeep Nema, John D. Ludwig

   This three-volume set of Pharmaceutical Dosage Forms: Parenteral Medications is an authoritative, comprehensive reference work on the formulation and manufacture of parenteral dosage forms, effectively balancing theoretical considerations with the practical aspects of their development. As such, it...

   Published December 14th 2012 by CRC Press
10. Pharmaceutical Formulation Development of Peptides and Proteins, Second Edition

    Edited by Lars Hovgaard, Sven Frokjaer, Marco van de Weert

    The rapid advances in recombinant DNA technology and the increasing availability of peptides and proteins with therapeutic potential are a challenge for pharmaceutical scientists who have to formulate these compounds as drug products. Pharmaceutical Formulation Development of Peptides and...

    Published November 13th 2012 by CRC Press