AU2003225834A1 – Improved Burner With Low Nox Emissions – Google Patents

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In June 1906, President Theodore Roosevelt signed into legislation the Pure Meals and Drug Act of 1906, additionally known because the “Wiley Act” after its chief advocate. The duty for analyzing meals and drugs for such “adulteration” or “misbranding” was given to Wiley’s USDA Bureau of Chemistry. In 1927, the Bureau of Chemistry’s regulatory powers were reorganized underneath a new USDA physique, the Food, Drug, and Insecticide Administration. Soon after passage of the 1938 Act, the FDA started to designate certain medicine as safe to be used solely under the supervision of a medical professional, and the category of “prescription-only” drugs was securely codified into legislation by the Durham-Humphrey Amendment in 1951. These developments confirmed in depth powers for the FDA to enforce post-advertising and marketing recalls of ineffective medication. Wiley used these new regulatory powers to pursue an aggressive marketing campaign towards the manufacturers of foods with chemical additives, but the Chemistry Bureau’s authority was soon checked by judicial decisions, which narrowly outlined the bureau’s powers and set high requirements for proof of fraudulent intent. By the thirties, muckraking journalists, client safety organizations, and federal regulators started mounting a marketing campaign for stronger regulatory authority by publicizing a listing of injurious products that had been ruled permissible under the 1906 legislation, including radioactive beverages, mascara that could cause blindness, and worthless “cures” for diabetes and tuberculosis.

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