Food And Drug Administration

Improved Essays
The U.S. Food and Drug Administration is one of the oldest extensive consumer protection agencies in the U.S. federal government. This independent regulatory agency all started back in 1848 when Lewis Caleb Beck ran chemical analyses of agricultural products. However, the FDA didn 't go by it’s present name until the 1930’s. FDA launched its new regulatory functions with the passage of the 1906 Pure Food and Drugs Act. This law strictly prohibited interstate commerce in adulterated and misbranded food and drugs. It’s safe to say that since 1906 the FDA has undergone some changes. Nevertheless, this administration’s mission statement stays the same: “Protecting and promoting your health.” The U.S. Food and Drug Administration is solely responsible …show more content…
Robert M. Califf, MD states that he, “is committed to strengthening programs and policies that enable the agency to carry out its mission to protect and promote the public health.” Before stepping into the roll of commissioner, Dr. Califf served as the Deputy Commissioner for Medical Products and Tobacco. Before the commissioner assumed any roll at the FDA, he was a professor of medicine and vice chancellor for clinical and translational research at Duke University. In addition, he also served as director of the Duke Translational Medicine Institute and founding director of the Duke Clinical Research …show more content…
Food and Drug Administration is a significantly important agency. Their main goal is protecting the public health of our nation. To learn more, one can go to their website. The administration’s website provided is easily navigated, quite informational, and professional and visually appealing. They have information on food recalls, outbreaks, and emergencies. In addition, they have adequate information on drug approvals and safety. The site is visually appealing and easily navigated with tabs specifically for each issue they deal with. Along with that, there are multiple links directing you towards other websites that will better ones understanding of certain dangers themselves and precautions to take. Although, the FDA’s website may be biased in the fact that they know what is best for peoples individual heath. In reality, there have been multiple drugs that have the FDA’s stamp of approval and then are recalled because they discover something new. Always remember that research is ongoing and just because the FDA approves something doesn 't mean its 100% safe in the long run. With that being said, the overall usefulness of the FDA and their website is twofold. In my opinion, the website is doing its job. For example, one could easily go to this site to be better educated on what exactly they 're putting in their

Related Documents

  • Improved Essays

    Cleanflo Case Study

    • 779 Words
    • 4 Pages

    The issue is whether the Cleanflo was sent to the hospital is a drug or not within the meaning of 21 U.S.C § 321 (p) of the act. According to 21 U.S.C § 321 (p), the term new drug means “(a) any drug (except a new animal drug or an animal feed bearing or containing a new animal drug) the composition of which is such that such drug is not generally recognized, among experts qualified by scientific training and experience to evaluate the safety and effectiveness of drugs, as safe and effective for use under the conditions prescribed, recommended, or suggested in the labeling thereof, except that such a drug not so recognized shall not be deemed to be a “new drug” if at any time prior to June 25, 1938, it was subject to the Food and Drugs Act…

    • 779 Words
    • 4 Pages
    Improved Essays
  • Superior Essays

    Another impressive achievement that he accomplished was The Pure Food and Drugs Act of 1906. The Food and Drug Act aims to protect consumers from bad food preparation procedures, false advertising, and drug addiction from medication. Meredith A. Hickmann stated, “The law sought to protect the consumer from being deceived or harmed, mainly by following a favorite assumption that the average man was prudent enough to plot his own course and would avoid risks if labeling made him aware of them” (21). This law requires food and drug companies to disclose all potential health risks to consumers when promoting their products. President Roosevelt signed two acts titled The Pure Food and Drugs Act and The Meat Inspection Act, which are both consumer protection laws that were created to protect consumer’s rights and safety.…

    • 1232 Words
    • 5 Pages
    Superior Essays
  • Improved Essays

    This will help build a great foundation for my professional pharmacist career. The FDA’s contribution to public health is not well understood to a lot of people. I actually only understood the FDA’s contribution to health care only after I started pharmacy school. I want to bridge this gap and learn more about the contribution of the FDA…

    • 557 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    The 1906: The Wiley Act

    • 389 Words
    • 2 Pages

    Prior to the 20th Century, there were few federal laws controlling the contents and sale of domestically produced food and medicine. Under Harvey Washington Wiley, 1883's chief chemist, the Department of Agriculture began conducting research into the safety of food and drugs in the American market. In 1906, President Theodore Roosevelt created the Food and Drug act, also known as the "Wiley Act", after Harvey Wiley. The FDA is part of the White House's Office of Regulatory Affairs, it is an agent inside the U.S. Department of Health and Human Services.. Since 1906, the FDA has evolved to better cater the needs of a larger nation, with economic, cultural, and political changes.…

    • 389 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Pharmaceutical companies, however, have found a simple way to beat the regulations and mandates of the FDA. It is called molecular modification, or “me-too” drugs (Klein, p.259, 2014). Drug companies take an existing drug that has met FDA testing and licensing and simply alter its molecular make up slightly. This allows the drug to be re-branded, re-named and re-sold as a brand new revolutionary drug. In fact, the drug is actually chemically the same as the previous drug it replaced.…

    • 2380 Words
    • 10 Pages
    Improved Essays
  • Improved Essays

    Food And Drugs Dbq

    • 1153 Words
    • 5 Pages

    In the late 19th and early 20th century people were beginning to pay attention to science and some used the science they were learning to look closer at the food and drugs that were distributed across the nation. As the scientists looked closer what they found was often deadly to whoever consumed it. These findings made people look at the industries the foods or drugs came from and found that corruption and greed was taking control. People were making shortcuts to get more money or poisoning people they needed out of their way and politicians often used this to their advantage so the companies were able to continue without fear of consequences. Eventually scientists started to fight the companies and tried to regulate the products which turned out to be harder than they anticipated.…

    • 1153 Words
    • 5 Pages
    Improved Essays
  • Improved Essays

    Opioids In America

    • 906 Words
    • 4 Pages

    When it comes to the regulation of drugs Americans are not informed fully on what the FDA’s actions are. Overall, their job is to ensure the drugs will not cause a large amount of harm but there is a large amount of science they do not test. Richard Deyo, an MD from The Journal of the American Board of Family Medicine, wrote an address that started the FDA’s procedures are lacking by that statement that, “It does not review advertisements before use, assess cost-effectiveness, or regulate surgery (except for devices). Many believe postmarketing surveillance of drugs and devices is inadequate” (Deyo). Important factors like cost-effectiveness are not accounted for which leave families who cannot afford alternatives.…

    • 906 Words
    • 4 Pages
    Improved Essays
  • Improved Essays

    Packages were required to have a label stating how much of these drugs were included in the preparation. For example, any generally sold “cures” for morphine dependency had to indicate that they contained another habit-forming drug. Basically, any drug could be sold and bought without federal restrictions as long as the ingredients were clearly listed on the label. By requiring a label, the public was exposed to the dangerous and addictive power of non-prescription medicine marketed in the country. This act specifically referred to alcohol, morphine, opium, cocaine, heroin, marijuana, and several other agents.…

    • 837 Words
    • 4 Pages
    Improved Essays
  • Decent Essays

    The role of pharmacologists are to perform research experiments to examine the effects of drugs and other substances on human health. They use findings to develop drugs to treat and prevent illnesses. According to the text, they work in research labs operated by hospitals, universities, drug companies, or other health-related organizations. Those who work in laboratories conduct research about the effects of drugs or chemicals on people and animals. The work of FDA pharmacologists can lead to regulations or bans on products that were designed for consumer use.…

    • 118 Words
    • 1 Pages
    Decent Essays
  • Great Essays

    At the end of the day when the clothes come off, how comfortable are you with your body? In Horace Miner’s satire of American life, he recognizes that, “The fundamental belief underlying the whole system appears to be that the human body is ugly…” (Miner); and with all the billboards, television ads, and magazines that project unrealistic photo-shopped standards of beauty, it is understandable why many members of society are obsessed with modifying their appearance. Society spends countless dollars on clothes, make-up, and numerous other beauty regimens, but what happens when all of our temporary tricks and tools no longer satisfy our desires to alter our appearance? From ritualistic to purely cosmetic, the act of body modification has transformed…

    • 2148 Words
    • 9 Pages
    Great Essays
  • Decent Essays

    FDA Food Modernization

    • 248 Words
    • 1 Pages

    The FDA Food Modernization Act of 2011 shifted the focus from responding to contamination to preventing it. This law requires preventive controls that are comprehensive and based on science, to be implemented in our food industry, instead of reacting to problems after they occur. First, this law allows the FDA to better protect public health by strengthening the food safety system. Some examples of how the FDA will do this is by having more access to records, protecting against adulterated food, and by reevaluating foodborne illness risks. Second, this act improves the capacity to detect and respond to food safety problems.…

    • 248 Words
    • 1 Pages
    Decent Essays
  • Decent Essays

    Under FDA regulations, facilities that manufacture, process, pack or hold food that is intended for human or animal consumption in the US must register with the FDA. Food businesses are also required to maintain certain records,…

    • 131 Words
    • 1 Pages
    Decent Essays
  • Superior Essays

    It is naïve to assume that the FDA is not influenced by politics, as it is a direct department of the government and ultimately under the power of the…

    • 1351 Words
    • 6 Pages
    Superior Essays
  • Improved Essays

    For many years, people living in China survived off a predominantly rice-based diet. However, if you think this is still the case today, think again. Over the years, China’s population has grown exponentially and today, it is a country that is supporting 1.3 billion people. With such a vast population, it isn’t a surprise that rice is no longer the highest-demanded food item in the nation. Today, China is consuming meat, dairy, produce and nut products faster than ever.…

    • 995 Words
    • 4 Pages
    Improved Essays
  • Improved Essays

    In Canada, the main regulator for pharmaceuticals is Health Canada. The counterpart in the United States is the Food and Drug Administration (FDA). The regulatory body is tasked with ensuring the…

    • 984 Words
    • 4 Pages
    Improved Essays