Comprehensive Guide to Toxicology in Preclinical Drug Development

Faqi, Ali S.

Other formats:

Book Information
Edition:	1st
Publisher:	Academic Press, Incorporated
ISBN:	0-12-387815-2 (0123878152)
ISBN-13:	978-0-12-387815-1 (9780123878151)
Binding:	Hardcover
Copyright:	2013
Publish Date:	11/12
Weight:	5.92 Lbs.
Pages:	885
Carton Quantity:	4
Subject Class:	PRM (Pharmacology)
Return Policy:	Returns accepted up to 90 days provided no other recalls or return restrictions apply.
Table Of Contents:	View
Contributing Authors:	View
ProQuest Ebook Central:	Available in ProQuest Ebook Central™ View

Class Specifications
Discipline:	Pharmacology
Subject Definition:	Drug Toxicity; Drug Discovery
NLM Class:	QV 600
LC Class:	RA1238
Abstract:	A Comprehensive Guide to Toxicology in Preclinical Drug Development is designed for toxicologists who need a thorough understanding of the drug development process. This multi-contributed reference will provide a detailed picture of the complex and highly interrelated activities of preclinical toxicology in both small molecules and biologics. Intended as a comprehensive resource for toxicologists in industry and regulatory settings, as well as directors working in contract resource organizations (CRO), this book will discuss discovery toxicology and the international guidelines for safety evaluation and present both traditional and nontraditional toxicology models. By incorporating the latest research in this area and featuring real-life examples and scenarios, this reference is a complete and practical guide to all aspects of preclinical drug testing. Chapters written by world-renowned contributors who are experts in their fields. Includes the latest research in preclinical drug testing and international guidelines. Covers preclinical toxicology in small molecules and biologics in one single source. Incorporates real-life case studies and examples and offers readers a practical resource that outlines day-to-day activities and experiences in preclinical toxicology.