Have you ever been in the grocery store and picked up a item and saw in the bottom corner, "FDA approved"? What is the FDA? Why do they approve stuff? Most importantly Why do they approve food? The Food and Drug Administration or for short, the FDA, is a federal agency of the united states department of Health and Human services, one of the United States federal executive departments. The Food and Drug Administration is responsible for protecting the public health by ensuring the safety, efficacy, and security of human veterinary drugs, biological products, and medical devices. They also ensure the safety of our nation's food supply, cosmetics, and products that emit radiation. The FDA was founded by Theodore Roosevelt and Harvey Washington
Regulating what the government should control and what they should not was one of the main arguments our founding fathers had to deal with when creating our nation, and to this day this regulation is one of the biggest issues in society. Yet, I doubt our founding fathers thought about the idea that the food industry could one day somewhat control our government, which is what we are now facing. Marion Nestles’ arguments in the book Food Politics: How the Food Industry Influences Nutrition and Health deal with how large food companies and government intertwine with one another. She uses many logical appeals and credible sources to make the audience understand the problem with this intermingling. In The Politics of Food author Geoffrey Cannon further discusses this fault but with more emotional appeals, by use of personal narratives. Together these writers make it dramatically understandable why this combination of the food industry and politics is such a lethal ordeal. However, in The Food Lobbyists, Harold D. Guither makes a different viewpoint on the food industry/government argument. In his text Guither speaks from a median unbiased standpoint, which allows the reader to determine his or her own opinions of the food industries impact on government, and vise versa.
The Prohibition or the Eighteenth Amendment was a huge failure for a law in 1920. There were many factors that led to its downfall that included illegal means, rise of gangsters, and the Twenty- First Amendment. Despite the Prohibition, it did not stop the people from drinking it and accessing it through thousands of speakeasies. It became a most lucrative business for criminals that led to dangerous competition. In 1933, the failed amendment was repealed and most people rejoiced that alcohol was legal again. The Eighteenth Amendment was an experiment that went horribly wrong and did absolutely nothing to bring any positive change. This was proof “that you don’t have to be drunk to come up with a really, really, bad idea.” (Carlson. 141)
The momentum generated by the passage of the Meat Inspection Act helped secure the passage of the Pure Food and Drug Act, which had been stalled in Congress since 1905. With these two pieces of legislation, the federal government took important steps to assure the public that the food they were eating met minimu...
To begin, the Federal Food and Drug Administration does not have the power to regulate supplements like it does with drugs. Once a product is out on the market, the FDA has to prove that it is dangerous or has illegal additives before it can be removed. The FDA has targeted around seventy tainted weight loss products after learning that they had been mixed with undeclared stimulants, diuretics, and antidepressants (Trebilcock 2). The Federal Food, and Drug, Administration is responsible for ensuring that the manufacturers of foods provide safe ingredients and the correct amount of dosages for their products.
The FDA stands for The Food and Drug Administration. The FDA is an agency of the
Every year approximately 200,000 souls die from prescription drug reactions, with another 80,000 dying from medical malpractice (The International). Where is the FDA based? Why do they continue to allow doctors to prescribe these drugs? How could they get to this point? What once was believed to be a panacia for depression has turned into Pandora's box (Tracy).
"Does FDA Require Animal Testing." Center for Food Safety & Applied Nutrition. 3 May 1999. 5 Dec. 2002. <http://vm.cfsan.fda.gov/~dms/qa-cos4.html>.
...ous tests (Law, 2004). They also must now have the FDA’s approval in order for a certain food or drug to be sold directly to consumers. Also the marketplace has changed, due to new ways to process the product in a more safe and effective manner. There were also changes due to political, economical, social, and cultural changes since 1906. In conclusion, the Food and Drug Act paved the way for the Progressive movement and food safety in America.
The Drug Enforcement Administration has many careers and responsibilities within the the entire agency. there are many different careers like Special agent, Diversion investigator, Intelligence research specialist, Forensic scientist, and Student/entry level positions. Theres a very big responsibility of the Drug Enforcement Administration and thats to Enforce laws on drugs and protect the people from harmful substances. Many harmful substances are getting out to the people everyday so the DEA must take actions against this threat to try and prevent or catch it before its to late. Many people try to get in with the DEA but its just as difficult as becoming a police officer now a days. There are many pros and cons to working for the Drug Enforcement Administration some good and some not so good.
FDAs public health protection duties. By ensuring that products and producers meet certain standards, FDA protects consumers and enables them to know what they are
as it does supporters. But, if we do not allow the Supreme Court to translate
In Lee Ann Fisher Baron’s “Junk Science,” she claims that the “food industry with the help of federal regulators” sometimes use “[a science that] bypasses [the] system of peer review. Presented directly to the public by…‘experts’ or ‘activists,’ often with little or no supporting evidence, this ‘junk science’ undermines the ability…[for] everyday consumers to make rational decisions” (921). Yet Americans still have a lot of faith in the U.S. Food and Drug Administration (FDA). According to a 2013 Pew Research study, 65% of Americans are “very favorable” or “mostly favorable” of the FDA. When it comes to what people put in their bodies, the FDA has a moral obligation to be truthful and transparent. The bottom line of the FDA’s myriad of responsibilities is to help protect the health of Americans. Deciding what to eat is a critical part of living healthily, and consumers must be able to trust that this massive government agency is informing them properly of the contents of food. While the FDA does an excellent job in many areas, it has flaws in other areas. One of its flaws is allowing the food industry to print food labels that are deceptive, unclear, or simply not true (known as misbranding). This is quite the hot topic because a Google search for “Should I trust food labels” returns well over 20 million results, many of which are blog posts from online writers begging their readers not to trust food labels. HowStuffWorks, a division of Discovery Communications, published an online article whose author claims that “[the food industry] will put what they want on labels. They know the game….” While the food industry is partially at blame for misbranding, the FDA is allowing it to happen. If a mother tells her children that it is oka...
The Pros and Cons of Drug Legalization Should drugs be legalized? Drugs are resources that are capable of affecting the American economy in many ways—both positively and negatively. Drugs often have a bad name, even though they help us everyday in medical cases. and the drugs with the worst reputations are not the most abused drugs. One may benefit from the legalization of drugs in many ways, while others would suffer greatly.
...ly look at the false claims made by food industries expand on their already set regulations, making it harder for companies to get around them. However, if the FDA believes that their regulations are as specific as they can get, then there should be at least somebody to educate consumers about food labels and add more detail to nutritional value charts. Because without changing the way how information is provided and educating people, they will not be able to change their diets to improve nations overall health.
Pharmaceutical patents are patents for inventions within the pharmaceutical industry. Patents give exclusive rights for an invention for a product or a process of making a product [1]. There are many aspects to patents in the pharmaceutical industry that are both pros and cons; it just depends on what industry you are in. Pharmaceutical companies take out patents so they can regulate the market and restrict competition from other companies. By obtaining patents pharmaceutical companies also attract investment. In addition to this pharmaceutical companies can also regulate the price of the drug as they will be the only company selling that drug. However these aspects of patents can adversely affect the generics industry. The generics industry cannot make or sell drugs that are patented but once a patent licence expires, both the generics industry and the WHO see increased benefits as drugs become more widely available around the world (i.e. developing countries) at a lower price. Here we will discuss the pros and cons of patents from the point of view of the pharmaceutical industry, generics industry and the WHO.