Analysis Of The Food And Drug Administration (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.

Food and drug administration is a department of U.S health and human services. It’s responsibility is to test the safety and efficacy of new drugs entering the market as well as to make sure that these medicines are quickly accessible to people. The Food, Drug, and Cosmetic Act has been passed in 1938 to ensure that foods other than meat, poultry and fish are clinically hygienic and safe to eat. This act also requires that the food should be labelled according to its content. (FDA.org) Drugs and tobacco are also regulated by FDA and in 1996, FDA strictly regulated the use of tobacco products like nicotine, cigarettes and smokeless tobacco, by children and adolescents because of the increase in diseases prevalence and tobacco addiction. Annually 40000 deaths are attributable to its use and most of them are of premature. Therefore the goal of FDA is to stop the tobacco addiction by minors and prevent the deaths and diseases due to nicotine addiction. (FDA vs Brown, n.d) This essay will cover the food and drug administration’s role in under and over regulating drugs and medicines and how it effects our economy, health care system and patients health and safety.

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

of food, drugs, and cosmetics. The day-to-day operations of the FDA occur within the Office of

The FDA also looks at several products that have chemical implications to them, such as drugs. It looks at drug manufacturing standards, as well as the labels of each drug (both over-the-counter and prescription drugs) and must give its approval on new drugs before they can be sold to the public. The FDA also looks at cosmetics. It must ensure that, like food articles, each product is properly labeled as to what comprises each item. Biological products, such as the nation’s blood supply, are also regulated by the FDA. It does research to improve upon the testing methods of blood, to ensure that the supply in hazard free. It also is in charge of handing out licenses to product and manufacturing establishments.

| Created the Food and Drug Administration (FDA). It forbids the manufacture or sale of adulterated or fraudulently labeled foods and drugs.

The Food and Drug Administration dates back to the late 1840s, though it did not adopt that name until 1930. The first act if the FDA as it is known today was officially established in 1906 with the passage of its first piece of legislature. was the passage of the 1906 pure food and drug act, which prohibited the interstate commerce of misbranded food and drugs, and thus establish the FDA . It was established by the government, and thus inherited sits bureaucratic structure. ome of its flaws . Furthermore , the FDA was established as a council to regulate agricultural products through chemical analysis, and thus its structure is incredibly flawed

At first I would gather information as possible as I can about the facts that let the company that I work for to avoid the FDA inspection. Then, I will define the ethical issues that let the company evade FDA inspection. When a company is doing that only to make profit at the customer’s expense. Also, without thinking about what will happen to the people whether harms will effect on their health or benefits which is rarely will happen. Moreover, if a customer gets harm that could affect the company production and its employees may lose their jobs. The values should a company has are responsibility, Integrity, and credibility. My obligation is to make sure the company’s product matches public safety standards and has the quality that will keep

It is the Food and Drug Administration’s (FDA) obligation to protect individuals in the United States from using and consuming harmful products.

Pharmaceutical products, medical devices, veterinary medicines and food supplements, all these products are subjected to regulations stated in the government policies to protect public health. All healthcare organisations or companies are constantly being monitored by a regulatory affairs department or commonly known as regulatory pharmacists to ensure their compliance with all the regulations and laws concerning their business. Regulatory pharmacists always adhere to ethical standards and refrain from abuses of power which make them true leaders who wield their power to achieve desired

Some of the programs include are PDUFA program that provides certain trainings to Scientists and physicians in using technologies to speed up the process of the trials. This program has cut the review time by 60% and also facilitate FDA in communicating with drug companies, while the approval is in process, to effectively identify drug developmental procedures. The FDA uses Fast Track, accelerated approval, priority review and expanded access programs to speed up the process of drugs testing, approval and availability. FDA is not alone in all these innovative findings. Many of the pharmaceutical companies are working hand on hand with FDA to provide patients access to life saving drugs. approaches to ensure foods safety. Many staff members including the scientists are involved with FDA in regulating the approval of safe and effective drugs. Several awards have been given to FDA scientists who have worked hard and performed well in their field of research. These awards include Excellence in Analytical Science Award , Excellence in Laboratory Science Award ,Excellence in Review Science Award,Lifetime Achievement Award, Outstanding Junior Investigator Award, Outstanding

In the United States, The Food and Drug Administration has the power to decide what is and is not safe to be consumed by the human body. The pharmaceutical industry makes billions a year, they develop, design, add chemicals to, and produce hundreds of new drugs a year. It has been argued by many scientists, economists, and average american citizens that the FDA regulates and approves of drugs based on biased opinions and for reasons other than the health of consumers.

The Central Government is concerned with laying down regulatory measures and standards for drugs, granting approval for the import or manufacture of new drugs and maintaining control over the quality of imported drugs.