The Food and Drug Administration Essay

The United States Food and Drug Administration is the government agency responsible for regulating food, dietary supplements, drugs, cosmetics, medical devices, biologics and blood products in the United States. The agency is authorized by the government to inspect, test, approve, and set safety standards for foods, chemicals, medical devices, cosmetics, and household devices (britanica.org). Made up of 2,100 scientist including chemists, pharmacologists, physicians, microbiologists, pharmacists, and lawyers, the FDA oversees the production of safe foods and the manufacturing of safe and effective drugs and is responsible in protecting the rights and safety of patients who are used in clinical trials for medical products. (allgov.com). They…

The U.S. Food and Drug Administration is one of the oldest extensive consumer protection agencies in the U.S. federal government. This independent regulatory agency all started back in 1848 when Lewis Caleb Beck ran chemical analyses of agricultural products. However, the FDA didn 't go by it’s present name until the 1930’s. FDA launched its new regulatory functions with the passage of the 1906 Pure Food and Drugs Act. This law strictly prohibited interstate commerce in adulterated and…

Government agencies are assigned a specific duty to perform. This helps the government work more efficiently because each agency has its own job. This prevents one given section of the government from being accountable for too many tasks. One such agency is the FDA. This acronym stands for Food and Drug Administration. As the name implies, they deal with regulating food and drug products. Although this is not all they do. The FDA also regulates tobacco products as well,…

The origin of The Food and Drug Administration can be traced in 1848 at the Patent Office, when Lewis Caleb Beck was examining chemicals in agricultural products. Yet, The Food and Drug Administration began with the passage of the 1906 Pure Food and Drugs Act. Upton Sinclair, Samuel Hopkins, and the Chief Chemist of the Bureau of Chemistry in the Department of Agriculture, Harvey Washington Wiley, were able to express the needs for the act in The Jungle. This final push was exactly what was…

The evolution of health care and pharmaceutical regulation in this country began prior to the creation of the Food and Drug Administration (FDA). Throughout history there have been key events that have occurred resulting in pivotal changes in health care regulation. From the formation of the FDA to the passing of the Patient Protection and Affordable Care Act (ACA), there has been a focus of safety and consumer protection as purpose for increased of health care regulation in United States.…

The need for a governmental body to ensure the safety of consumers from food and drug products brought about the creation of the Food and Drug Administration (FDA). Since 1906 the FDA has played a key role in regulating essential products such as seafood, vegetable produce, food, additives, drugs, and even tobacco products to some extent. Programs like HACCP (Hazard Analysis Critical Control Point) ensures food safety through verification procedures throughout production. For drug regulation,…

The Food and Drug Administration Big markets need standards to achieve success. Otherwise, without substantial control, markets fail due to poor quality. The bad quality of food and drugs may result in the death or illness of people. In 1937, a drug called Elixir Sulfanilamide poisoned and caused 100 deaths in the US which led to the passing of The Food and Drug Administration Act of 1938. The Food and Drug Administration works to minimize the adverse effects of food and drugs. Likewise, the…

The Food and Drug Administration, established June 30th 1906 by Theodore Roosevelt and Harvey Washington Wiley, is an essential part of our federal government. It began after the Food and Drug act was passed in 1906. It was intended to regulate misbranded food and drugs (The History of FDA's Fight for Consumer Protection and Public Health) and has evolved into what it is now, regulating everything from food to supplements to cosmetics to pacemakers. The FDA consists of one commissioner and…

proper care services are provided. Regulation of all health care here in the U.S has been under the umbrella of the Department of Health and Human Services There are various regulatory agencies that monitor these health care facilities such as Occupational Safety and Health Administration (OSHA), Centers for Medicare and Medicaid Services (CMS), Food and Drug Administration (FDA) to ensure established rules and regulations are adhered to (HCA – 460 lecture 3). The regulating agency to be…

more effective. The U.S. Congress creates laws and instructs federal agencies like the Food and Drug Administration to carry them out and regulate industries ("U.S. Food and Drug Administration"). There are 2 major laws, enacted in 1938 and 1966, which govern the cosmetics industry: the Federal Food, Drug, and Cosmetic Act (FD&C Act) and the Fair Packaging and Labeling Act (FPLA) (Cosmeticsinfo.org). The FD&C Act defines adulterated and misbranded products and illegalizes such products for sale…