The Food And Drug Administration Is A Regulatory Agency Responsible For The Public Health Of American Residents Essay

The FDA has come a long way since 1906, but in my opinion, I believe that the FDA should do more to protect our health and have stricter laws in place concerning our food and medicines. The FDA allows products to be on the market without prior approval; for the FDA to take action and recall a product something awful like multiple deaths have to happen for them to realize that the product is harmful. Prime example, Red #3 is food coloring that FDA permits in our food to make the food look appealing. However, studies done on animals have proven to show that Red #3 causes cancer. According to an article published in 1990 in the New York Times states that "Red Dye No. 3 still has some approved uses in foods and drugs, but the F.D.A. said it is

The Food and Drug Administration (FDA) is best known for its role on protecting the health of the public by making sure that food, medications are safe and effective. Especially when it comes to the pharmaceutical industry, its mission is to regulate pharmaceutical manufacturers, as well as the drug approval process. However, in the recent years, many arguments and controversy regarding drug development and regulation have risen. Drug advertisements make false and misleading claims, products are being put out on the market without any proof of safety, causing many unwanted incidents such as the Avandia incident and Vioxx incident, which could have been prevented in the first place.

The Food and Drug Administration, also known as the FDA or USFDA, is responsible for protecting and advocating public health. They are the official government agency that ensures our drug supply is safe and effective. This is achieved through the regulation and supervision of food safety, dietary supplements, veterinary products, cosmetics, vaccines, biopharmaceuticals, medical devices, prescription and pharmaceutical drugs that can be purchased over- the- counter.

The FDA is something that many people know about, but do not know what happens within the company. A majority of Americans have heard stories on the news of people making huge acquisitions of how the FDA killed their child by no correctly regulation fast food companies ; or how their husband died for a heart attack because the warning label on his bottle of medication was not correct.

The Federal Food, Drug Administration is responsible for establishing the Code of Federal Regulations which outlines the rules and regulations governing pharmaceuticals. The rules are divided into sections and include guidance based on drug categories. Due to each person having varying reactions to pharmaceutical products not all side-effects are detected during clinical testing. The Federal Food, Drug Administration is responsible for sharing the information with consumers. However, it seems a bit unethical because the large pharmaceutical companies do not have to share all of side-effect information that may assist consumers in making its choice on whether to try a product or to not try a product. Through various survey’s it was discovered that consumers are under the opinion that pharmaceutical companies need to have improved internal controls to ensure their compliance with regulations. Due to physicians and pharmaceutical companies working together and are dependent on one another there needs to be controls in place that would have an unbiased view of the regulations. The government will need to continue introducing new regulations that will aide in monitoring the relationships.

The Food & Drug Administration became a possibility because of the Pure Food and Drugs Act of 1906. Harvey Washington Wiley was the driving force behind this law and headed its enforcement, which provided basic elements of protection that consumers had never had before (FDA's Origin). The FDA is an agency that works within the US Department of Health and Human Services of the executive branch of government (About FDA). The Food and Drug Administration is responsible for protecting the public health of all Americans by ensuring the safety, efficacy, and security of a large range of products from drugs to cosmetics (What We Do).

The FDA is and agency that falls into the Department of Health and Human Services under the Executive Branch, probably the most interesting agency in my eyes because of its importance in the nation and how a mistake from them or maybe a wrong move can be lethal. This very important agency can actually be traced back to the 1800's but bills were placed after it earlier agencies to become what it is today after protests and cries of those living in the nation around the early 1900's. (Office of the Commissioner) Its food we are talking about and food is something we insert into our body including the drugs we take. Therefore, it involves with our daily lives and with them being around it can protect us form the threats of health out there.

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 United States Food and Drug Administration, also known as the FDA, is the government agency “responsible for protecting the public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological product, medical devices, our nation’s food supply, cosmetics, and product that emit radiation.” It is “also responsible for advancing the public health by helping to speed innovations that make medicines more effective, safer, and more affordable. Created under the Theodore Roosevelt administration under the 1906 Pure Food and Drugs Act, the FDA still operates as a part of the federal bureaucracy. What if the very institution supposed to be looking out for the public health and advancement of medical

A terrible incident happened in Tennessee in 1937 when a drug called Elixir Sulfanilamide was mislabeled and contained toxic quantities of antifreeze that killed over 100 people (FDA's Origin & Functions - FDA History). Before this event, Congress debated substituting the 1906 Act and this instance in Tennessee drove Congress to approve the Food, Drug and Cosmetic Act of 1938 that provided an updated set of standards. Unlike before when the government had to disprove a drug was effective, the new act stated that drugs had to be proven effective before being sold. It not only replaced the Pure Food and Durg Act, but the Sherley Amendment as well (Centennial Edition of FDA Consumer).

To understand when, how and who began the Food and Drug Administration, one must trace it back to 1848 and to a man named Lewis Caleb Beck. In 1848, Beck was appointed to the Patent Office, to perform chemical analyses of agricultural products; later this function was passed on to the Department of Agriculture in 1862, which was the beginning of the Bureau of Chemistry, the predecessor of the Food and Drug Administration. In 1930, the Bureau of Chemistry changed its name to FDA, and today it serves under the Department of Health and Human Services. In 1883, Dr. Harvey W. Wiley became the chief chemist at the Bureau and he immediately increased the food adulteration studies; which was the beginning of an uphill battle for law changes in the

The United States of America is arguably the greatest country in the history of the world. With this great global influence, one could assume the United States ensures the best for its citizens health and prosperity, to be a role model for the rest of the world. However, you would be greatly surprised. The United States is failing to take action against some of the major immoralities committed by its own bureaucracies, which consistently cause detrimental harm to the well-being of the American public. A significant bureaucracy that is responsible for a great deal of harm to the U.S. is the Food and Drug Administration, or FDA. The FDA is preventing the sustainability of the

Every day as American's go about their lives, most do so with out the cumbersome worry of their food safety. It is because of the Food and Drug Administration that we are able to enjoy such a freedom that many around the world are lacking. Unfortunately, the FDA is ill equipped to meet the needs of a market that is continually expanding. The 400 inspectors that the FDA currently employs are unable to keep up in a market that has doubled in the last decade. Despite new discoveries in food preservation, the FDA simply cannot keep stride with the daunting task of assuring public food safety. Armed with this knowledge, companies are finding that they can simply disregard governmental regulations, as the odds are

As the years, products, and medical advancements progress so has regulations, but what surprised me is that these tragedies that had to be the means of creating the FDA to what it is today. The first event that was mentioned was the public outcry regarding the chemical foods and phony medications that were being sold. In discovery of the way these necessities for the population were being handled it made me think that those handling the products were all about the money. I understand that things happen and they were trying to accommodate more people, or better products but of you see a problem address it, it’s disappointing in learning the facts about these issues, and how they were not address until the people demanded a change.

On a regular basis, consumers like you and I buy items everyday not knowing the total chemicals that are in them. We trust that cosmetic products we buy everyday will be safe, but there are ingredients in our daily products that could or has caused conditions that we don’t know of. In 1820, the very first meeting the U.S had gathered physicians to create regulations on drugs in the United States. The general purpose of The FDA was to have a standard on the drugs that were being imported into the United States. It wasn’t until 1848 the Drug Importation Act was passed by Congress. It required U.S. Customs Service inspection to stop entry of adulterated drugs from overseas. In the middle of 1906, 58 years later the food and drugs act was passed. The original Food and Drugs Act was passed by Congress on June 30 and signed by President Theodore Roosevelt. It prohibits interstate commerce in misbranded and adulterated foods, drinks and drugs (FDA).