Food and Drug Law: Federal Regulation of Drugs, Biologics, Medical Devices, Foods, Dietary Supplements, Cosmetics, Veterinary and Tobacco Products is a title that aims to make a complex area of federal regulatory law easier to understand. Organized into twelve volumes, there is a separate volume for each subject based on regulation under the United States Federal Food, Drug and Cosmetic Act (FDCA) and related laws.
The 2015 eighth edition of Food and Drug Law Includes:
- Top United States Supreme Court cases
- Latest laws and regulations
- Latest issues
- FDA and beyond
Get your copy of the go-to resource for any practitioner, librarian, attorney, academia, or government personnel who works with food and drug law before the end of the year!
View the complete brochure here
About the Author
Roseann B. Termini, Esq., has thirty years of extensive experience in food and drug law. Further, she has published on a broad array of specialized food and drug law issues such as corporate accountability, criminal liability, enforcement, health claims, supplements, safety, duty to warn, preemption, regulation, promotion, tobacco, stem cells, risk assessment and globalization. She was the first awardee of the Plain English Award. Termini initiated the inaugural online food and drug law courses at Widener University School of Law and the direct-to-consumer promotion at St. Joseph’s University executive program. She served as the sole corporate counsel for an FDA-regulated company and senior deputy attorney general, Pennsylvania Office of Attorney General. Besides her professional association committee appointments, she was selected to serve on the President’s Council at Immaculata University, served as Food and Drug Law Institute Committee Chair, and is a member of the Central Atlantic Association of Food and Drug Law Officials.
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Item #: 1000110
Published: FORTI Publications, 2015
Distributed: William S. Hein & Co., Inc.