Preclinical Development Handbook, 2 Volume Set: Toxicology / Adme and Biopharmaceutical Properties: 11 (Pharmaceutical Development Series) - Hardcover

Hardcover

ISBN 10: 0471213837 ISBN 13: 9780471213833

Publisher: Wiley-Interscience, 2008

Synopsis

This book brings together in one resource an overview of the preclinical process along with a compendium of methods and techniques that need to be considered when developing a new drug. The book details steps in the preclinical process including: prioritizing and optimizing leads, dose formulation, ADME, pharmacokinetics, toxicity, modeling, and regulations. It includes problems that are encountered, solutions to these problems, and limitations of various methods and techniques used in determining the safety and efficacy of a drug at this stage.

About this title

About the Author

Shayne Cox Gad, PHD, DABT, ATS, is the Principal of Gad Consulting Services. He has more than thirty years of experience as a toxicologist, statistical consultant, manager, and consultant on research and development in the chemical, consumer product, contract testing, biotechnology, medical device, and pharmaceutical industries. He is the author of twenty-nine books and numerous papers, presentations, and other publications.

Edition details

• Publisher: Wiley-Interscience
• Publication date: 2008
• Language: English
• ISBN 10: 0471213837
• ISBN 13: 9780471213833
• Binding: Hardcover
• Edition number: 1
• Number of pages: 2432
• Editor: Gad Shayne Cox