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Title 21 is the portion of the Code of Federal Regulations that governs food and drugs within the United States for the Food and Drug Administration (FDA), the Drug Enforcement Administration (DEA), and the Office of National Drug Control Policy (ONDCP). [1] It is divided into three chapters: Chapter I — Food and Drug Administration
The Pure Food and Drug Act of 1906 was the first of a series of significant consumer protection laws enacted by the Federal Government in the twentieth century and led to the creation of the Food and Drug Administration. Its main purpose was to ban foreign and interstate traffic in adulterated or mislabeled food and drug products, and it ...
In June 1906, President Theodore Roosevelt signed into law the Pure Food and Drug Act, also known as the "Wiley Act" after its chief advocate. [1] The Act prohibited, under penalty of seizure of goods, the interstate transport of food which had been "adulterated," with that term referring to the addition of fillers of reduced "quality or strength," coloring to conceal "damage or inferiority ...
Swann, John P. "History of the FDA." The Food and Drug Administration. Hauppauge: Nova Science, 2003. 9-16. Wax, Paul M. "Elixirs, Diluents, and the Passage of the 1938 Federal Food, Drug and Cosmetic Act." History of Medicine 122 (1995): 456-61. Young, James H. "The Long Struggle for 1906 Law." The Food and Drug Administration.
Charges against the owner were filled, and six months later, a law called the Food, Drug, and Cosmetic Act of 1938 was signed. This law forced all new food, drugs, and cosmetics to be certified by the FDA before being put on the market. [17] This act granted the FDA with enforcing and legal power that has helped regulate food and drugs ever since.
21 U.S.C. ch. 9 — Federal Food, Drug, and Cosmetic Act 21 U.S.C. ch. 10 — Poultry and Poultry Products Inspection Poultry Products Inspection Act of 1957
The Food and Drug Administration Safety and Innovation Act of 2012 (FDASIA) is a piece of American regulatory legislation signed into law on July 9, 2012.It gives the United States Food and Drug Administration (FDA) the authority to collect user fees from the medical industry to fund reviews of innovator drugs, medical devices, generic drugs and biosimilar biologics.
The law of Virginia consists of several levels of legal rules, including constitutional, statutory, regulatory, case law, and local laws. The Code of Virginia contains the codified legislation that define the general statutory laws for the Commonwealth.