Development and Evaluation of Drugs:From Laboratory through Licensure to Market

Description

Features:
�Updates and expands on the information provided in the previous edition
�Discusses hot topics such as genome structures, rational drug design, good manufacturing practices, and more
�Covers bioavailability and bioequivalence and their importance to drug manufacturers
�Provides detailed regulatory information for critical phases of drug development pre-licensure, and post-marketing (Phase IV) studies
Development and Evaluation of Drugs has been used as a textbook and reference for scientists in biomedical research, industry, and regulatory agencies. Updated and expanded, this second edition examines recent advances in scientific and regulatory approaches as well as changes in the way in which drugs are discovered, developed, and evaluated. The information provided outlines critical steps beginning from drug discovery in the laboratory to licensure and approval for market.

Biomedical research is an intrinsically changing and evolving field. A more direct strategy for drug discovery has gradually replaced random screening of natural products. More rapid identification of key molecular structures for new drug candidates and characterization of biomolecules including proteins, polysaccharides, and nucleic acids are now possible. The ability to chemically modify cell surfaces and carbohydrate linkages has facilitated designs of the next generation of new drugs.
Thoroughly discussing these issues and more, Development and Evaluation of Drugs focuses on the la developments in the science and regulation of bringing new drugs to market, including activities of the International Commission on Harmonization.
Contents
1. Introduction
2. Drug Evaluation from Laboratory through Licensure to Pharmacist’s Shelf
3. Practical Aspects of Drug Evaluation and Response
4. Development of New Drugs by Research Institutes and the Pharmaceutical Industry
5. Challenging Problems in the Future

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