Good Manufacturing Practice (GMP) Guidelines: The Rules Governing Medicinal Products in the European Union EudraLex Volume 4 Concise Reference

Good Manufacturing Practice (GMP) Guidelines: The Rules Governing Medicinal Products in the European Union EudraLex Volume 4 Concise Reference

by Mindy J. Allport-Settle
     
 

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This title combines all of the human and veterinary Regulations, Directives and guidance for medicinal products used by the pharmaceutical industry as their main source when manufacturing and distributing medicinal products in the European Union.  See more details below

Overview

This title combines all of the human and veterinary Regulations, Directives and guidance for medicinal products used by the pharmaceutical industry as their main source when manufacturing and distributing medicinal products in the European Union.

Product Details

ISBN-13:
9780982147603
Publisher:
PharmaLogika
Publication date:
12/28/2009
Pages:
686
Product dimensions:
6.00(w) x 9.00(h) x 1.37(d)
Age Range:
18 Years

Meet the Author

Mindy Allport-Settle has served as a key executive, board member, and consultant for some of the best companies in the pharmaceutical, medical device, and biotechnology industry. She has provided guidance in regulatory compliance, corporate structuring, restructuring and turnarounds, new drug submissions, research & development and product commercialization strategies, operational, project and contract management, and new business development. Her experience and dedication have resulted in international recognition as the developer of the only FDA-recognized and benchmarked quality systems training and development business methodology. Her education includes a Bachelor's degree from the University of North Carolina, an MBA in Global Management from the University of Phoenix, and completion of the corporate governance course series in audit committees, compensation committees, and board effectiveness at Harvard Business School.

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