Food And Drug Administration Act Of 1938

Good Essays
The Food and Drug Administration

Big markets need standards to achieve success. Otherwise, without substantial control, markets fail due to poor quality. The bad quality of food and drugs may result in the death or illness of people. In 1937, a drug called Elixir Sulfanilamide poisoned and caused 100 deaths in the US which led to the passing of The Food and Drug Administration Act of 1938. The Food and Drug Administration works to minimize the adverse effects of food and drugs. Likewise, the FDA ensures the true labeling of foods and drugs on the market. The FDA focus on the drugs, food, medical devices, and cosmetics.

It is important to control drugs on markets because of the high potential of abuse. The drug abuse may lead to the death

Related Documents

  • Decent Essays

    During the 19th and 20th century pharmaceutical researchers didn’t have enough resources to test out medications. The lack or resources lead to a high number of health disasters. In the 1930s more than a dozen woman went blind when they used a mascara that contained a chemical that could burn the skin. One of the women effected, conditions were so bad that she died from an infection. In 1937 a pharmaceutical agent named diethylene glycol (DEG) wasn’t tested, which led to a lot of deaths. A company…

    • 206 Words
    • 1 Pages
    Decent Essays
  • Amazing Essays

    following questions: • Briefly explain what the FDA is, it’s mission, and how it achieves its mission. FDA (U.S. Food & Drugs Administration): It is a federal administration which protects the safety and public health of the U.S. The mission of the FDA is to ensure the safety of every American family by ensuring the control and the potency of the products offered to the population, such as food supply, cosmetics, medical devices, medications, and others. Also, the goals are to provide obtainable and secured…

    • 1687 Words
    • 7 Pages
    Amazing Essays
  • Good Essays

    RANBAXY DRUG-ADULTERATION CONTROVERSY The Food, Drug and Cosmetic Act of United States (abbreviated as FDCA) is a set of laws passed by Congress in 1938 giving authority to the Food and Drug Administration (FDA) of the country to oversee the safety of food, drugs, and cosmetics. As per the act: A drug is adulterated if the methods used in or the facilities or controls used for its manufacturing, processing, packing or holding do not conform to or are not operated or administered in conformity with…

    • 687 Words
    • 3 Pages
    Good Essays