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The Pure Food and Drug Act of 1906, also known as Dr. Wiley 's Law, was the first of a series of significant consumer protection laws which was enacted by Congress in the 20th century and led to the creation of the Food and Drug Administration.
Pure Food and Drug Act, in U.S. history, legislation passed in 1906 to ensure the sanitary preparation of consumable goods. The Pure Food and Drug Act required accurate ingredient labeling and prohibited the sale of adulterated and misbranded food and drugs in interstate commerce.
23 de may. de 2018 · PURE FOOD AND DRUG ACT. June 30, 1906, was a red-letter day for those who sought progressive reform and consumer protection in the United States. On that date the U.S. government passed the Pure Food and Drug Act, the first in a series of legislation designed to regulate the quality of food and pharmaceutical products.
The Pure Food and Drug Act of 1906 prohibited the sale of misbranded or adulterated food and drugs in interstate commerce and laid a foundation for the nation’s first consumer protection agency, the Food and Drug Administration (FDA).
The Food and Drugs Act, June 30, 1906: A Study with Text of the Act, Annotated, the Rules and Regulations for the Enforcement of the Act, Food Inspection, Decisions and Official Food Standards. Washington, D.C.: J. Byrne & Company.
30 de ene. de 2023 · Milestones in U.S. Food and Drug Law. From the beginnings of civilization people have been concerned about the quality and safety of foods and medicines. In 1202, King John of England...
1 de jul. de 2014 · Summary and Definition: The Pure Food and Drug Act (PFDA) prohibited the interstate transportation and sale of impure, contaminated food. The law was an important element of Roosevelt's Square Deal Domestic Policy and an important piece of legislation during the history of the Progressive Era.