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Preclinical Drug Development (Drugs and the Pharmaceutical Sciences Volume 152)

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Subject
Science
ISBN
9781574448825
Publication Year
2005
Series
Drugs and the Pharmaceutical Sciences Ser.
Type
Textbook
Format
Hardcover
Language
English
Publication Name
Preclin Drg Deve
Author
Rogge Markc., Taft David
Item Length
9in
Publisher
CRC Press LLC
Item Width
6in
Item Weight
36.1 Oz
Number of Pages
600 Pages

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Product Information

This reference discusses in detail the broad realm of preclinical drug development. Topics range from assessment of pharmacology and toxicology through the regulatory expectations that support clinical trials. Providing chapters on pharmacokinetics, modeling and simulation, formulation and routes of administration, toxicity evaluations, the assessment of drug absorption and metabolism, and interspecies scaling, this guide is a fundamental resource for medicinal chemists, biologists, and other specialists in the drug development sciences.

Product Identifiers

Publisher
CRC Press LLC
ISBN-10
157444882x
ISBN-13
9781574448825
eBay Product ID (ePID)
14038626816

Product Key Features

Author
Rogge Markc., Taft David
Publication Name
Preclin Drg Deve
Format
Hardcover
Language
English
Publication Year
2005
Series
Drugs and the Pharmaceutical Sciences Ser.
Type
Textbook
Number of Pages
600 Pages

Dimensions

Item Length
9in
Item Width
6in
Item Weight
36.1 Oz

Additional Product Features

Series Volume Number
152
Lc Classification Number
Rm301.25.P745 2005
Table of Content
The Scope of Preclinical Drug Development: An Introduction and Framework. Interspecies Differences in Physiology and Pharmacology: Extrapolating Preclinical Data to Human Populations. Transgenic Animals for Preclinical Drug Development. Pharmacokinetics/ADME of Small Molecules. Pharmacokinetics/ADME of Large Molecules. Preclinical Pharmacokinetic-Pharmacodynamic Modeling and Simulation. Formulation and Route of Administration - Influencing Drug. Assessment of Pharmacokinetics and Drug Activity: Isolated Organ. Alternate Methods for Assessing Absorption, Metabolism and Routes of Toxicity Evaluations: ICH Guidelines and Current Practice. Application of Pathology in Safety Assessment. Principles of Toxicogenomics: Implications for Preclinical Drug Development. Utilizing the Preclinical Database to Support Clinical Drug Development
Copyright Date
2005
Topic
Pharmacology
Lccn
2005-048422
Dewey Decimal
615/.19
Intended Audience
Scholarly & Professional
Dewey Edition
22
Illustrated
Yes
Genre
Medical

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