This 2017 comprehensive “Go to Resource” Food and Drug Law new edition book contains all 12 Volumes with up to date information to guide those in this complicated field of law and covers FDA and beyond. This valuable “All-in-One” reference tool is for government, industry and the academic community.
Volume I: The “Why” of the United States Food and Drug Administration, Landmark Laws and Court Decisions
Volume II: Food and Drug Law Administrative Primer
Volume III: Criminal and Civil Enforcement Strategies
Volume IV: Medical Device and Radiation Emitting Products Regulation
Volume V: Human Drug Regulation–Approvals, Promotion, Marketing, Warnings, Accountability, and Postmarket Surveillance
Volume VI: Biotechnology and Biologic Products Regulation
Volume VII: Veterinary Products Regulation
Volume VIII: Personal Care Products Regulation
Volume IX: Food Regulation—Food Safety, Recalls, Claims, Additives, Allergens, and Biotechnology
Volume X: Dietary Supplement, Herbs, and Botanicals Regulation
Volume XI: Tobacco Products Regulation
Volume XII: Product Classification, Politics, Foreign Corrupt Practices and Globalization
Food and Drug Law is also available as 12 separate subject-specific E-Books.
2017 Published $180.89
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