New Drug, Antibiotic, and Biological Drug Product Regulations; Accelerated Approval; Final Rule
Federal Register. 1992 Dec 11; 57(239): 58942-58960.
Showing items related by title, author, creator and subject.
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 creator (United States. Food and Drug Administration [FDA], 2006-01-24)