Fda's Food Codes

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 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.

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

FDA stands for Food and Drug Administration, it is responsible for protecting the public health by assuring that foods are

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:

A job of the FDA is ensuring the safety of the nations food and drug products. One way they do it with food is by having manufactures send a report of the process that it takes to make the food so they can see if the process is a healthy or unhealthy one. The FDA do 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.

What is the FDA and what does it do you may ask? The FDA stands for Food and Drug Administration. They are responsible for protecting the public’s health, and ensure the safety and security of human and veterinary dugs. They also regulate the making, selling and distribution of products. The FDA regulates many things including foods, like additives and supplements, drugs, both prescription and non-prescription, biologics, like vaccines and blood products,

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

FDA is a very important organization to inspect all food additives. FDA stands for Food and Drug Administration. It oversees a variety of products involving food, drugs, cosmetics, animal food, dietary supplements, medical devices, biological goods and blood products. It is the agency in the United States Department of Health and Human Services. Protecting public health is a key priority of the FDA. Safety concerns prompt the FDA to pull one to two drugs and six to eight food and medical devices from the market annually. It is the FDA’s duty to address serious risks that can be avoided and managed. The FDA reviews the safety and effectiveness of food and medical

The Food and Drug Administration was founded in 1906, through President Roosevelt. FDA is an agency part of the Department of Health. It was founded for the propose of protecting the public health, so that people were safe. FDA also helped to make sure that the production of cosmetics were under regulation and safe. Also it was used to help the consumers to get the best possible information they needed to help them safely choose their medicines and foods to help improve their health. Through the checking of meat, safety of medical devices, and nutrition information labeled on products, the FDA has helped people make sure the products people are using are safe to use and consume.

This article fits nicely with our current topic, The Bureaucracy, because it demonstrates the power of the Executive Cabinet. The FDA, which resides under the Health and Human Services department, has the ability to discern between what products can be released for general consumption and, as a brief analysis of its role, ultimately determines whether a product can be sold.