Labeling Products of Biotechnology: Towards Communication and Consent
Journal of Agricultural and Environmental Ethics 2000; 12(3): 319-330
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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)