Preview

Food And Drug Administration

Good Essays
Open Document
Open Document
526 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Food And Drug Administration
The Federal Agency I am choosing is Food and Drug Administration or FDA for short. The FDA is a Federal Agency of the United States Department of Health and Human Services. This Federal Agency is part of the Executive Departments. This Administration was founded on June 30, 1906 and the founders were Theodore Roosevelt and Harvey Washington Wiley. Some of the Subsidiaries are Center for Drug

Evaluation and Research,Center for Food Safety and Applied Nutrition, and National Center for Toxicological Research. This Agency was founded because of the Pure Food and Drug Act in 1906. The Pure Food and Drug Act was a law and it removed harmful foods and drugs. The responsibilities of the FDA was that it wanted to protect the public from harmful things that can harm the public. The FDA is an important part of the Federal Agency and the United States. The FDA is an important part of the federal government agency and United States.
…show more content…
The Center for Drug Evaluation and Research(C.D.E.R) is a division of the U.S. Food and Drug Administration that keeps an eye on most drugs as defined in the Drug, Food, and Cosmetic Act. The The Center for Food Safety and Applied Nutrition(C.D.F.A.N) is part of the division is part of the agency because it regulates the food, and dietary supplements. The National Center for Toxicological Research(N.C.T.R) is also apart of the FDA because it does research to define biological mechanisms of toxicity of products. Each of these is apart of the FDA and prevents any harm to the public. They are doing their job and keeping the public

You May Also Find These Documents Helpful

  • Satisfactory Essays

    11. A firm that works with the Food and Drug Administration to create new regulations is practicing:…

    • 483 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    As the outbreaks occurred, the US Food and Drug Administration (FDA) collaborated with other federal agencies and health officials in investigating the outbreaks to gather information with people who got sick to see what could possibly prevented the illness. They will also supervise closely to determine if all restaurants are safe and can be…

    • 390 Words
    • 2 Pages
    Good Essays
  • Satisfactory Essays

    Cross 9e TBB Ch24

    • 2356 Words
    • 12 Pages

    The Consumer Product Safety Commission is the primary agency that issues regulations on food labeling.…

    • 2356 Words
    • 12 Pages
    Satisfactory Essays
  • Satisfactory Essays

    In 1906, our country enforced the Pure Food and Drug Act. It pushed drug companies to remove medicines that were not scientifically tested. That was only one of the many ways our country help improve food safety.…

    • 71 Words
    • 1 Page
    Satisfactory Essays
  • Satisfactory Essays

    Hcs/ 490 Outline

    • 475 Words
    • 2 Pages

    References: Division of Drug Marketing, Advertising, and Communications (DDMAC). 2010. Retrieved August 6, 2010 from http://www.fda.gov/AboutFDA/CentersOffices/CDER/ucm090142.htm Food and Drug Administration (2010). Division of Drug, Marketing, Advertising, and Communications. Retrieved from http://www.fda.gov/AboutFDA/CentersOffices/CDER/ucm090142.htm Us Food and Drug Administration. (2010). Retrieved August 9, 2010 from website: http://www.fda.gov/AboutFDA/WhatWeDo/default.htm US Food and Drug Administration (2010). “Inspection, Compliance, Enforcement and Criminal Investigations.” Retrieved August 16, 2010 from www.hhs.gov.…

    • 475 Words
    • 2 Pages
    Satisfactory Essays
  • Better Essays

    Palcohol Final

    • 1738 Words
    • 2 Pages

    release and letter to a commissioner to] call on the Food and Drug Administration (FDA) to step in and…

    • 1738 Words
    • 2 Pages
    Better 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
  • 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
  • Better Essays

    Sherman Act Of 1890

    • 1119 Words
    • 5 Pages

    The FDA, esatblished in 1906, regulates the safety and effectiveness of food, drugs, and cosmetics. The EEOC, established in 1964, regulates the hiring, firing, and promotion of workers. OSHA, established in 1971, regulates industrial health and safety. The EPA, established in 1972, regulates air, water, and noise pollution. The CPSC, established in 1972 as well, regulates the safety of consumer products (McConnell, Brue, Flynn, 2011, pg.…

    • 1119 Words
    • 5 Pages
    Better Essays
  • Powerful Essays

    Communication Coordinator

    • 1323 Words
    • 6 Pages

    The U.S. Drug and Food Administration’s Center for Drug Evaluation and Research (CDER), is a unit responsible for validating that all drugs marketed in the United States are safe and effective (FDA, 2010). According to the Food and Drug Administration, “CDER does not test drugs, although the Center's Office of Testing and Research does conduct limited research in the areas of drug quality, safety, and effectiveness” (FDA, 2010). To market a medication to the public and health care establishments, Essie Pharmaceuticals…

    • 1323 Words
    • 6 Pages
    Powerful Essays
  • Good Essays

    The Bioterrorism Act directed the U.S. Food and Drug Administration, also known as the FDA, to implement regulations for the registration of food facilities; prior notice of imported food shipments; the establishment, maintenance and availability of records; and the administrative detention of food for human or…

    • 416 Words
    • 2 Pages
    Good Essays
  • Good Essays

    First, I will test the drug to make sure it is safe and effective for its intended use. A team of CDER physicians, statisticians, chemists, pharmacologists, and other scientists reviews the company's data and proposed labeling. If this independent and unbiased review establishes that a drug's health benefits outweigh its known risks, the drug is approved for sale. The center will not actually test the drugs, although it does conduct limited research in the areas of drug quality, safety, and effectiveness standards.…

    • 729 Words
    • 3 Pages
    Good Essays
  • Powerful Essays

    Health Law Regulation

    • 1164 Words
    • 4 Pages

    US Department of Health and Human Services. (2013, May 6). What does FDA regulate? Retrieved March 8, 2014, from US Department of Health and Human Services: http://www.fda.gov/aboutfda/transparency/basics/ucm194879.htm…

    • 1164 Words
    • 4 Pages
    Powerful Essays
  • Good Essays

    I am a Multifaceted individual with varied experience of pharmaceutical and healthcare industry.With the current innovation and integration of medicine, technology and business, a need for increased regulatory compliance is imperative to ensure that reliable and safe products are available to the public so that we may continue to lead healthy lives.Currently working in pharmacovigilance as a domain trainer and drug safety scientist my expertise include Pharmacovigilance, Drug Safety, Regulatory Affairs, QA and QC.…

    • 730 Words
    • 3 Pages
    Good Essays
  • Satisfactory Essays

    jfgdh

    • 502 Words
    • 3 Pages

    Food and drug administration (FDA)-Federal agency that was formed to set and enforce safety standards for food, drugs, and cosmetics.They have the authority to stop the sale of an item under their jurisdiction, if it is found to be harmful or hazardous.They may also require safety warnings to be placed on harmful or hazardous products.This is the agency which tests new drugs and medications before they are put on the market.…

    • 502 Words
    • 3 Pages
    Satisfactory Essays