Preview

The Pros And Cons Of The FDA

Satisfactory Essays
Open Document
Open Document
265 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
The Pros And Cons Of The FDA
The FDA helps advance public health by speeding up product innovations. The public is informed with science-based in, Puerto Rico formation needed to use medicines, foods and devices to improve their health ( UDHHS, 2010). The FDA approval process not only makes sure that the product's ingredients are safe but also that labels show all ingredients and do not make unverified claims. This has caused the FDA symbol to now become one that consumers trust(Gelinas, 2010).
FDA’s Jurisdictions
How far does the FDA’s authority expand?
The FDA’s has authority over the 50 United States, Guam, the Virgin Islands, the District of Columbia, American Samoa, Puerto Rico and other U.S. territories (Gelinas, 2010)
The FDA ensures the safety of prescription

You May Also Find These Documents Helpful

  • Good Essays

    I would be writing about interest groups and bureaucracy. The FDA bureaucracy article in a way stresses the importance or impact of the executive agency in carrying out its functions. I find testing how politicians try to sway the FDA (and other administrative agencies) in a way to suit their purpose is both necessary and may have a potential for undermining the administration. I thought the research question is of high importance; being able to test the efficiency (in terms of timeliness and quality of outcomes) of an administrative agency using the FDA as a case study. While different agencies will have their peculiarities, it is still necessary to be able to assess them this way. A drawback to this test could be something entirely unrelated…

    • 666 Words
    • 3 Pages
    Good 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
  • Powerful Essays

    Imagine that you are at work and suddenly your head begins throbbing and you just can’t concentrate or focus on your tasks any longer. You take a quick ride to the corner store and grab a bottle of Tylenol™, toss a handful back with some bottled water and return to work. 30 minutes later you are keeled over with stomach pains and feelings of nausea, chills and fever all at the same time. This miserable experience is the onset of acetaminophen overdose. Commonly used over-the-counter pain medications such as Tylenol™, Motrin™ or Advil™ carry potential dangers, risks and long-term side effects of which many people…

    • 1540 Words
    • 7 Pages
    Powerful Essays
  • Satisfactory Essays

    Fda Pros And Cons

    • 72 Words
    • 1 Page

    With reference to your e-mail please note that we only requested from your side to send us the correct ROE page as per the request of our client.…

    • 72 Words
    • 1 Page
    Satisfactory Essays
  • Satisfactory Essays

    The way I chose to use this small amount of information is to inform the reader of the tasks which the FDA claims to tackle. I focused specifically on the very first talking point about the protection of public health by assuring that foods are safe, sanitary, and properly labeled as I will be referring to sanitary and labels in the essay as well. This source, albeit short, was actually very helpful at introducing the reader to the talking points that will be covered throughout the paper and as a result the source was used fairly early into it. The first bullet was quoted to demonstrate to the reader that it seems that the FDA is a filter for us and prevents any products that deemed unsafe from food manufacturers. Which immediately leads to…

    • 190 Words
    • 1 Page
    Satisfactory Essays
  • Good Essays

    DVX Pro Liquid

    • 681 Words
    • 3 Pages

    A major problem in the field of health and nutrition is a law passed in congress called the Dietary Supplement Health and Education Act of 1994, or DSHEA. This law essentially requires the Food and Drug Administration to assume that dietary supplements are safe until proved otherwise. Making supplements used to be like making prescription drugs, you had to prove your product was safe and effective before you could sell them. Since DSHEA was passed, the supplement industry has become a multi-billion dollar business with manufacturers free to make all sorts of grandiose claims for their products and even include ingredients that are harmful to the consumer’s health.…

    • 681 Words
    • 3 Pages
    Good Essays
  • Satisfactory Essays

    The Food and Drug Administration (FDA) agency is the federal agency of the United States Department of Health and Human Services. FDA is responsible to protect public health by promising quality, efficacy, and safety of human and veterinary drugs, medical devices, food supply, cosmetics and any other products that release radiation (FDA Lecture PowerPoint). FDA is also responsible for assuring the security of food supply and its emerging effects on human health.…

    • 72 Words
    • 1 Page
    Satisfactory Essays
  • Good Essays

    Editorial Analysis

    • 622 Words
    • 3 Pages

    This article does not specially call its audience to action, however it does raise awareness in its readers. The article reminds its readers of other slip-up’s from the FDA’s poor inspection quality and limited action to reduce the occurrences of poisoning.…

    • 622 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Dietary Supplements Paper

    • 762 Words
    • 4 Pages

    This label is a standard label similar to the Nutrition Facts label for foods and also usually has the words dietary supplement on the label (Grosvenor, 2006). The FDA has authority to collect information on supplement safety and they are able to remove a product from the market if the FDA can prove that the product carries significant risk (Grosvenor, 2006). For example, the FDA exercised its right to remove products containing Ephedra from the market place (Grosvenor, 2006). The FDA found that products with Ephedra were linked to one hundred-fifty-five deaths and dozens of heart attacks and strokes (Grosvenor, 2006). The FDA has also found other ingredients to be hazardous and asked that they voluntarily remove the ingredients. Although the FDA is able to set regulations surrounding dietary supplements there are no mandatory standards in manufacturing supplements therefore the amount of an ingredient in a dietary supplement and how well it is absorbed in a person’s body varies from dose to dose (Grosvenor,…

    • 762 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Once the FDA has reviewed a chemical and believes it is safe to consume the product is marked as GRAS, which means generally recognized as safe. According to Nelter and Maffini in the article, Generally Recognized as Secret: Chemicals Added to Food in the United States, studies across the world have proved that additives marked as GRAS had opposing results. (9-10) The four main additives done in the study were Epigallocatechin-3-gallate, Theobromine,…

    • 1649 Words
    • 7 Pages
    Good Essays
  • Better Essays

    There are so many products out in the market with big labels claiming to do amazing miracles, but just aims at getting money out of your pocket. Science has developed a lot and we need to keep up with it and start understanding the facts rather than just keeping up with the beliefs. FDA is putting every single effort to make sure that the citizens consume a better product. We need to have faith in them and appreciate the work they are putting in. If an event takes place, first look onto the scientific side of that, why did it occurred and then make any assumptions rather than straight away assuming that it happened because of another event taking place somewhere. Believe me you will save a lot of money which you are spending on these ineffective products, and will be remaining healthy and secure of the side-effects of these…

    • 1218 Words
    • 5 Pages
    Better Essays
  • Powerful Essays

    Jim Maryanski from the U.S. Food and Drug Administration, had the following to say in an interview published on the FDA's website.…

    • 2277 Words
    • 7 Pages
    Powerful Essays
  • Better Essays

    Ensure the company provides detailed product info. These information must be evaluated by the FDA. This detail includes a comprehensive list of product ingredients, the quality and expiration and a list of what it is expected to heal, cure or treat.…

    • 943 Words
    • 4 Pages
    Better Essays
  • Powerful Essays

    Before a medical device or a drug can enter the market, there are strict rules and regulations that must be met. Prior to passed government regulations, adequate research must be completed in order to…

    • 2620 Words
    • 7 Pages
    Powerful Essays

Related Topics