Changes in Protocol Requirements for Researchers and Prescription Requirements for Practitioners
FEDERAL REGISTER 50(202): 42184-42187, 18 October 1985
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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)