Preview

History of Fda

Powerful Essays
Open Document
Open Document
2705 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
History of Fda
History of the FDA

From a staff of one to over 9,000, the Food and Drug Administration has seen great changes since it was first created in 1862. Stemming from a single chemist in the U.S. Department of agriculture, the FDA now encompasses most food products, both human and animal drugs, cosmetics and animal feed. The FDA received it start under a different name. First called the Division of Chemistry, which played a small part in everyday life, then in July of 1901, the name was again changed to the Bureau of Chemistry. The FDA that we now know came from the passage of a bill in 1906, the Federal Food and Drug Act shaped the role that the FDA would come to play. The bill gave the FDA its power to regulate over a wide subject matter. In 1927 the name was again changed from the Bureau of Chemistry to the Food, Drug and Insecticide Administration. Once again, in 1930 the name was changed, it was now called the FDA and still had all of its original power. The Depart of Agriculture controlled the FDA, and then its power was shifted to Federal Security Agency. In the year of 1953, the FDA was again transferred to the Department of Health, Education and Welfare. Today the FDA currently sits within the Department of Public Health Services, still a part of the HEW. The power that the FDA has comes from its ability to regulate and control. The FDA has its own set of laws that it regulates. The ultimate control of the FDA comes from the way in which the courts view and interpret their regulations. Before the creation of the FDA, the power to regulate was given to the states. This caused many problems as each state has different rules and regulations. The federal government did little to nothing in the way is controlled the distribution of Food and Drugs. The makers of consumer drugs had no control over their product and where often undercut by makers of cheaper, less potent drugs. The same issue happened with food where there was no control of the way that food was

You May Also Find These Documents Helpful

  • Satisfactory Essays

    The Food and Drug Administration has the power to force businesses that make or sell defective products to take corrective action.…

    • 1126 Words
    • 8 Pages
    Satisfactory Essays
  • Good Essays

    NEHA STUDY GUIDE

    • 2196 Words
    • 8 Pages

    You come to work and find stock left in sink at room temperature, what should you do?…

    • 2196 Words
    • 8 Pages
    Good Essays
  • Powerful Essays

    Ethics Chp4. Exam Review

    • 2324 Words
    • 10 Pages

    The _____ regulates tobacco, dietary supplements, vaccines, veterinary drugs, medical devices, cosmetics, products that give off radiation, and biological products.…

    • 2324 Words
    • 10 Pages
    Powerful Essays
  • Good Essays

    - The FDA is responsible for keeping the public healthy by making sure that the nation’s food supply is clean, clearly and honestly labeled, and healthy for whoever eats it.…

    • 676 Words
    • 3 Pages
    Good Essays
  • Better Essays

    Hcs/430 Regulatory Agency

    • 1496 Words
    • 6 Pages

    The role and responsibility of the U.S. Food and Drug Administration (FDA), most importantly, is to uphold the laws dictated by the government concerning products that include drugs, medical products, food, and non-health related products and to protect and promote public health across the country. This essay focuses on several aspects of the FDA, from the role of the agency and its effect on health care in the United States, to the authority this agency carries in relation to health care. There will also be an explanation of how the FDA carries out these responsibilities on a day-to-day basis. The FDA has held a strong presence in the realm of public health since 1848 when it began as a consumer protection agency (FDA, 2013). The FDA, formed after the 1906 Pure Food and Drug Act was put in place and inspired by the scientific work of Harvey Washington Wiley, who was the Chief Chemist at the U.S. Department of Agriculture. Wiley worked to eliminate the dangerous practices of marketing unregulated drugs and food products to consumers (FDA, 2013). Since that time, the FDA has become a powerful force, monitoring and working to protect public health in the United States.…

    • 1496 Words
    • 6 Pages
    Better Essays
  • Satisfactory Essays

    Nt1310 Unit 2 Study Guide

    • 3091 Words
    • 13 Pages

    How do some regulatory agencies function as providers of healthcare and as healthcare regulatory agencies?…

    • 3091 Words
    • 13 Pages
    Satisfactory Essays
  • Better Essays

    Fda Research Paper

    • 2368 Words
    • 10 Pages

    The Food and Drug Administration started in 1906 with the passage of the Pure Food and Drugs Act. Use of poisons coupled with poor conditions in meat packing plants causing people to become ill prompted the government to create a regulatory agency to protect the safety of Americans (Howland, 2008). Before the introduction of regulation, consumers had no way of knowing if the food and medications they purchased were safe or effective. According to Howland (2008), during the early 1900s cure-all claims for ineffective and possibly dangerous patent medications was normal. While this was a good start in…

    • 2368 Words
    • 10 Pages
    Better Essays
  • Good Essays

    DBQ: The Progressive Era

    • 782 Words
    • 4 Pages

    protected the nation's food supply. The Pure Food and Drug Act was also passed and provided…

    • 782 Words
    • 4 Pages
    Good Essays
  • Good Essays

    The Federal Food, Drug, and Cosmetic Act (FFDC) can be found in chapter 9 of title 21 in the United States Code. Congress passed the act in 1938, in effort to protect the well being of the country by controlling the food and medical supply at a federal level. The act permitted the Food and Drug Administration (FDA) to have the authority to carry out legislative obligations. Specifically, the FDA enforced standards that limited the maximum amount of residue levels for unavoidable poisonous substances on food due to pesticides. The FDA website claims to have established laws that provided three types of food standards. These standards include: standard of identity, standard of quality, and standard of regulating the fill of container. Any food that did not meet these FDA standards would be, “misbranded.” The Act also regulates the pharmaceutical industry to guarantee the safety and effectiveness of drugs manufactured and retailed in the United States. (http://www.fda.gov/AboutFDA/WhatWeDo/History/ProductRegulation/ucm132818.htm)…

    • 1575 Words
    • 7 Pages
    Good Essays
  • Satisfactory Essays

    perhaps, the government society and more. The FDA, in this specific case, comes in to find out…

    • 260 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Dr. Harvey Analysis

    • 816 Words
    • 4 Pages

    Historians debate as to what the motives were of Dr. Harvey in campaigning for the 1906 laws and what purpose of the Pure Food and Drug Act was. Hunter Dupree stated that Wiley’s motives weren't to act out of pure selflessness, and loyalty to the public. Wiley pushed for reforms in the food and drug regulation via his adulteration of foods to save his Division of Chemistry, which Wiley thought was going to come to an end due to the large government agencies that were hiring their own private chemists (9, 277). Richard Hofstadter thought that the act was an example of the shift from the concern of the producer, to the concern of the consumer. Robert Wiebe saw the act as an example of experiment in bureaucratic reform. Conflict also arose about…

    • 816 Words
    • 4 Pages
    Good Essays
  • Better Essays

    The CVM’s main role is to protect both the animal’s and the public health by regulating veterinary medicine and medicated feed. Regulation of animals before they are sold to the public for consumption is also a priority that falls to the CVM. It can be argued that the FDA is protecting animals by regulating feed and what they are getting for medications and vaccines. In turn, this increases the quality of the feed with more valuable nutrition than if it were unregulated; causing less health problems than food that is not being inspected and meeting FDA requirements. By not using unnecessary medications, there would be less of a risk of drug resistance. On the other side of the discussion, you could argue that although the FDA may have a specific organization working towards regulating animal drugs and medicated feed, their main goal is to maintain public health. They have regulations on food, but only to the point where it does not specifically harm the animals. In their eyes, as long as it doesn’t cause illness or death to the animal or the public who may be ingesting the animal, it is good…

    • 952 Words
    • 4 Pages
    Better Essays
  • Good Essays

    * McDonalds doesn’t follow FDA standards, the FDA is an agency of the US Department of Health and Human Services.…

    • 942 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Along with foods in the United States, they must check foods coming into or leaving the United States for proper food labeling and that the food is safe for consumption. It is important that food venders/ sellers or distributors are sure of all FDA laws before selling their foods, for they could be fined or put in jail for bad food labeling or unsafe foods. The NLEA act says that all foods sold and brought into the United States must have the proper food labeling and nutrition facts to be legally sold in the United States. Food industries often change their food labels because of frequent changes in the laws that are required for food labeling. The FDA must keep up to date on nutrition facts and proper food labeling or something will go…

    • 902 Words
    • 4 Pages
    Good Essays
  • Good Essays

    The FDA is only trying to do what is best Americans by fighting to ban antibiotics from animal feed. Although our livestock producers disagree and believe that it would be cheaper to use antibiotics in our animal feed, our health is more important. The bottom line is this isn’t something that should be ignored voluntary bans are a positive step forward in dealing with this…

    • 333 Words
    • 2 Pages
    Good Essays