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Hace 1 día · The Pure Food and Drug Act was then passed by the United States Congress in 1906 and required that certain special drugs, including cannabis, be accurately labeled with contents. Previously, many drugs had been sold as patent medicines with secret ingredients or misleading labels. [14]
Hace 6 días · May 28, 1906: Foreign Dredge Act of 1906; June 8, 1906: Antiquities Act; June 29, 1906: Hepburn Act; June 30, 1906: Pure Food and Drug Act of 1906 (Wiley Act), ch. 3915, 34 Stat. 768; June 30, 1906: Meat Inspection Act (Beveridge Act) 1906: The Carnegie Foundation for the Advancement of Teaching chartered.
Hace 4 días · First known as the Food, Drug, and Insecticide Administration when it was formed as a separate law enforcement agency in 1927, the FDA derives the greater part of its regulatory power from four laws: the Federal Food, Drug, and Cosmetic Act, which established safety and purity standards and provided for factory inspection and for ...
Hace 5 días · A bill to amend the Federal Food, Drug, and Cosmetic Act to allow manufacturers and sponsors of a drug to use alternative testing methods to animal testing to investigate the safety and effectiveness of a drug, and for other purposes. In GovTrack.us, a database of bills in the U.S. Congress.
Hace 3 días · As a result of the outrage provoked by the novel, Progressive reformers pushed through the Meat Inspection and Pure Food and Drug Acts of 1906; these institutions later evolved into the Food and Drug Administration and were a major victory for proponents of industrial regulation and consumer protection. " ...
Hace 5 días · Jul 9, 2012. S. 3187 (112th). A bill to amend the Federal Food, Drug, and Cosmetic Act to revise and extend the user-fee programs for prescription drugs and medical devices, to establish user-fee programs for generic drugs and biosimilars, and for other purposes. In GovTrack.us, a database of bills in the U.S. Congress.
Hace 5 días · Like foods and unlike drugs, no government approval is required to make or sell dietary supplements; the manufacturer confirms the safety of dietary supplements but the government does not; and rather than requiring risk–benefit analysis to prove that the product can be sold like a drug, such assessment is only used by the FDA to decide that a dietary supplement is unsafe and should be ...
