Federal Food, Drug, and Cosmetic Act: The United States Federal FD&C Act Concise Reference by Allport-Settle, Mindy J.

Federal Food, Drug, and Cosmetic Act: The United States Federal FD&C Act Concise Reference (Paperback) (ISBN-13: 9780983071907)

Vendor: Mindy J. Allport-Settle
Product type: Books
Format: Paperback
$48.99
$48.99
$48.99
Subtotal: $48.99
Federal Food, Drug, and Cosmetic Act: The United States Federal FD&C Act Concise Reference by Allport-Settle, Mindy J.

Federal Food, Drug, and Cosmetic Act: The United States Federal FD&C Act Concise Reference

$48.99
Federal Food, Drug, and Cosmetic Act: The United States Federal FD&C Act Concise Reference by Allport-Settle, Mindy J.

Federal Food, Drug, and Cosmetic Act: The United States Federal FD&C Act Concise Reference

$48.99
Format: Paperback
Description
Description
x
This book is designed to be a unified reference source for the U.S. Federal Food, Drug, and Cosmetic Act and is designed to be used both as a reference for experienced industry representatives and as a training resource for those new to the industry. Federal Food, Drug, and Cosmetic Act: * Introduction to the FDA and the FD&C Act * Part I: Federal Food, Drug, and Cosmetic Act o Section Number Reference: Federal Food, Drug, and Cosmetic Act o FD&C Act Chapters I and II: Short Title and Definitions o FD&C Act Chapter III: Prohibited Acts and Penalties o FD&C Act Chapter IV: FoodFD&C Act Chapter V: Drugs and Devices o FD&C Act Chapter VI: Cosmetics o FD&C Act Chapter VII: General Authority o FD&C Act Chapter VIII: Imports and Exports o FD&C Act Chapter IX: MiscellaneousSignificant Amendments to the FD&C Act Reference Tools * Part II: Combined Glossary and Index for all Regulations

Author: Mindy J. Allport-Settle
ISBN-10: 098307190X
ISBN-13: 9780983071907
Publisher: Pharmalogika
Language: English
Published: 10/13/2010
Pages: 672
Format: Paperback
Weight: 2.50lbs
Size: 9.25h x 7.52w x 1.35d
By Mindy J. Allport-Settle
By Mindy J. Allport-Settle
x
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 and development, 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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