Preclinical Development Handbook
Edited by Shayne C. Gad
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Preclinical Development Handbook by Shayne C. Gad
Book DescriptionThis 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.
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Book DetailsISBN: 9780471213833
(258mm x 186mm x 98mm)
Imprint: Wiley-Blackwell (an imprint of John Wiley & Sons Ltd)
Publisher: John Wiley and Sons Ltd
Publish Date: 16-Apr-2008
Country of Publication: United Kingdom
Books By Author Shayne C. Gad
Development of Therapeutic Agents Handbook, Hardback (January 2012)
This book is a one-stop compendium of up-to-date concepts, approaches, methodologies, and limitations in drug development and therapeutics. It provides researchers with a thorough reference focusing on applications, practical methods, and techniques to facilitate new drug development.
Drug Discovery Bundle, Hardback (November 2011)
This multi-volume set comprises all the handbooks in Shayne Gad's comprehensive and authoritative Pharmaceutical Development Series.
Clinical Trials Handbook, Hardback (May 2008)» View all books by Shayne C. Gad
Provides a comprehensive and thorough reference on the basics and practices of clinical trials Includes chapters on hot topics like: adverse event reporting (AER) systems, adaptive trial designs, and crossover trial designs Presents chapters on issues for specific disease areas: cardiology, oncology, cognitive, dermatology, etc.
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