The Federal Food, Drug, and Cosmetic Act requires the premarket approval of new drugs prior to their marketing. FDA accomplishes this through regulations that establish Investigational New Drug Applications (INDs) and New Drug Application (NDAs).
CITATION STYLE
Reuter, N. (1999). FDA Regulation of Prescription of Controlled Substances. In Marihuana and Medicine (pp. 751–755). Humana Press. https://doi.org/10.1007/978-1-59259-710-9_75
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