Outline of the History of U.S. Drug Regulation and Labeling
Janssen, Wallace F.
Food, Drug, Cosmetic Law Journal 1981 August; 36(8): 420-441
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Requirements on Content and Format of Labeling for Human Prescription Drug and Biological Products and Draft Guidances and Two Guidances for Industry on the Content and Format of Labeling for Human Prescription Drug and Biological Products; Final Rule and Notices Unknown author (United States. Food and Drug Administration [FDA], 2006-01-24)