Politics Has Too Much Influence on the FDA

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 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 Food and Drug Administration has an important role in keeping people healthy. They dictate food labeling and quality control of the food that reaches grocery store shelves. Along with overseeing safe food practices, they control what medications are brought to the public. When a new drug is brought to the FDA, they will test it extensively before allowing

The FDA’s regulations would impact the food and drug production industries in multiple ways. Firstly, the regulation decreased the quantity of goods that the companies had available to sell. For example, before the Pure Food and Drug Act, meat-packing companies could pack and sell deceased animal meat, like from dead cattle. The sum of the dead

The FDA received it start under a different name. First called the Division of Chemistry, which played a small part in everyday life, then in July of 1901, the name was again changed to the Bureau of Chemistry. The FDA that we now know came from the passage of a bill in 1906, the Federal Food and Drug Act shaped the role that the FDA would come to play. The bill gave the FDA its power to regulate over a wide subject matter.

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).

The Food and Drug Administration (FDA) is a division of the Department of Health and Human Services (HHS) and received its name in 1930. Although the FDA’s roots can be traced back as far as 1862, its right as a regulatory agency came into effect under the 1906 Pure Food and Drugs Act. This legislation was created to eliminate misrepresentation of food and drugs in an effort to protect the health of the public. Over the years, the FDA’s role has further evolved to overseeing many areas other than just food and drugs. However, its mission has remained the same:

There was a time where there was no limits to what substances were in products we humans consume or use everyday. It is alarming to think that there could be items in our food or medicine that are potentially dangerous and deadly. It is for these reasons that the Food and Drug Administration came to be. It all started in a time where companies could say anything they wanted about a product without any scientific validation or proof. The government stepped in and established the Pure Food and Drugs Act of 1906 along with a new agency: the FDA. This act's purpose was to protect the public against dangerous substances in food and from products identified as healthy without scientific support. This law was an accumulation of many bills and ideas that aimed to protect consumers from contaminated products. (The Pure Food and Drug Act) Now, the FDA conducts recalls, market withdraws, and safety alerts in order to protect the citizens.

The Food and Drug Administration is a regulatory agency responsible for the public health of American residents. The agency is located in Silver Springs, Maryland. The current extent of FDA regulations reaches a wide variety of product groups such as electronic devices, cosmetics, foods, biologics, tobacco, medical devices, and veterinary devices (US Food & Drug Administration, 2016). The FDA is also accountable for the safety of the food supply, prescription drugs, and the manufacturing of products such as tobacco (US Food & Drug Administration, 2016). The FDA’s organization is divided into five offices: office of the commissioner, foods and veterinary medicine, medical products and tobacco, global regulatory operations and policy, and operations (FDA Organization, 2016). According to the FDA website, the President’s 2016 fiscal year FDA budget is 4.9 billion dollars (2016 FDA Budget Summary, 2016).

The FDA is responsible for protecting the public health by assuring the safety, effectiveness, quality and security of human and veterinary

The U.S. Food and Drug Administration (FDA) is the governmental division that protects the public’s health by guaranteeing food, drugs, and medical devices are safe and effective. It assures that dietary supplements and cosmetics are well labeled, regulates tobacco, protects the users from electronic product radiation, among others.

The FDA behaves in ways that enhance its reputation for protecting consumer safety and public health. As gauged by public opinion polls, the FDA remains one of the most popular agencies in government, regularly securing 70 percent or greater “approval” of its performance among sampled respondents.5 Buttressing this popularity are powerful symbolic lessons of history: The FDA is widely credited with saving thousands of American lives in its response to the sulfanilamide tragedy of 1937 and the thalidomide scandal of 1959–1961.6 Congress dramatically strengthened pharmaceutical regulations after each of these events. Thereby whether or not the agency deserves it, the FDA clearly possesses a reputation for protecting public health and consumer safety.