Food and Drug Administration

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    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 misbranded food and drugs. It’s safe to say that since 1906 the FDA has undergone some changes. Nevertheless, this administration’s mission statement stays the same: “Protecting and promoting your health.” The U.S. Food and Drug Administration is solely responsible…

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    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…

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    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,…

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    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.…

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    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…

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    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,…

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    The U.S. Food and Drug Administration (FDA) is among the primary federal agencies responsible for developing public health regulations. It is the agency, which has duty to protect the nation’s food supply. It is the FDA to make sure the safety of the food in both major franchise store and small fast food establishment. Rules and Regulation¬¬; Food Handling As a preventative step, the FDA wants that every fast food and restaurant workers to complete a food handling course. That course is…

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    use products to protect one’s skin to the effects of age and sun damage. A licensed esthetician is a professional who utilizes skilled techniques with the use of cosmetic products for each client. The following sections will describe the importance of understanding the differences between consumer use products and professional use products in association with their regulations in the United States of America. As a licensed esthetician, the federal government regulates many products for the…

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    The antioxidant typically found in green tea is called EGCG short for Epigallocatechin Gallate. When caffeine and green tea extracts are combined, the effect on weight loss is small. The United States Pharmacopeia is a nonprofit organization that sets standards for dietary supplements. These standards are enforced by the Food and Drug Administration. According to the United States Pharmacopeia, Green tea extracts have been probable causes in seven cases and a possible 27 other cases of liver…

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    Bacteria are becoming more resistant to these pharmaceutically manufactured antibiotics and bacteria have been shown to mutate making antibiotics less effective. In addition, pharmaceutically manufactured antibiotics can interfere with other medications and make them less effective. For example, people on certain cholesterol medications are recommended to avoid using clarithromycin and erythromycin because it can reduce the effect of the drugs used as their cholesterol regimen (Dr. Mercola,…

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