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by Mindy J. Allport-Settle (Author)
FDA Acronyms, Abbreviations and Terminology provides a quick reference to the acronyms, abbreviations and definitions related to Food and Drug Administration (FDA) human and veterinary products regulatory activities. The emphasis for this reference guide is on scientific, regulatory, government agency, computer application terms, and includes some FDA organizational and program acronyms. Definitions from Title 21 of the United States Code have been included because of their relevance to FDA activities.
Author Biography
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 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.
