Food and Drug Administration

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  • The Food And Drug Administration

    1204 Words  | 5 Pages

    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

  • The Food And Drug Administration

    1928 Words  | 8 Pages

    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

  • The Food And Drug Administration

    1902 Words  | 8 Pages

    In 2008, the Food and Drug Administration (FDA) approved the use of Moxatag, a once daily extended release formulation of amoxicillin, for the treatment of streptococcal pharyngitis. The clinical study results indicated that Moxatag was as safe and effective as penicillin V, the first drug of choice for the treatment of pharyngitis (Infectious Disease Society of America, 2013). Moxatag is the only once daily medication FDA approved for the treatment of pharyngitis. The manufacturer claims that

  • The Food And Drug Administration

    1834 Words  | 8 Pages

    The Food and Drug Administration (FDA) is responsible for protecting and promoting public health through regulating pharmaceutical drugs, biologics and medical device in context to granting approvals for marketing authorization, surveillance of the clinical trial study of the drug, post-marketing surveillance of the medical product, etc. The Pharmaceutical companies seek for FDA approval for a new drug to be marketed through a long process. This process starts with applying an application known

  • The Flawed Food And Drug Administration

    1805 Words  | 8 Pages

    Bennett Ms. Romine ENG 1010 4 December 2015 The Flawed Food and Drug Administration 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

  • Food And Drug Administration: The FDA

    445 Words  | 2 Pages

    To begin we will be discussing the federal Agency called food and drugs administration better known as FDA. As a federal agency the FDA has a lot of responsibility with regulating food and drug safety. The FDA works to provide good medical services and insured food products. The FDA works to support our country so that we can live peacefully and healthily but they don't just stop there they wish to help other countries and have even expanded there work to other countries such as China and Costa

  • The Food And Drug Administration Essay

    848 Words  | 4 Pages

    The Food and Drug Administration (FDA) is responsible for protecting and promoting public health through regulating pharmaceutical drugs, biologics and medical device in context to granting approvals for marketing authorization, surveillance of the clinical trial study of the drug, post-marketing surveillance of the medical product, etc. The Pharmaceutical companies seek for FDA approval for a new drug to be marketed through a long process. This process starts with applying an application known

  • U.s. Food And Drug Administration

    3715 Words  | 15 Pages

    U.S. Food and Drug Administration Proposed Rule to Extend Its Reigns Over E-Cigarettes Abstract 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

  • Food And Drug Administration ( Fda )

    871 Words  | 4 Pages

    According to the US Food and Drug Administration (FDA), the definition of a drug includes the following; “a substance recognized by an official pharmacopoeia or formulary. A substance intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease. A substance (other than food) intended to affect the structure or any function of the body. A substance intended for use as a component of a medicine, but not a device or a component, part or accessory of a device. Biological products

  • The Food and Drug Administration Essay

    866 Words  | 4 Pages

    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. When a pharmaceutical company

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