Food and Drug Administration (redirect from FDA)
Food and Drug Administration (FDA or US FDA) is a federal agency of the Department of Health and Human Services. The FDA is responsible for protecting...
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Look up FDA in Wiktionary, the free dictionary. FDA or Food and Drug Administration, is an agency responsible for the control and safety of food and drugs...
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Commissioner of Food and Drugs (redirect from FDA commissioner)
commissioner of food and drugs is the head of the Food and Drug Administration (FDA), an agency of the United States Department of Health and Human Services...
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Criticism of the Food and Drug Administration (redirect from Criticism of the FDA)
excessive and/or insufficient regulation. The U.S. Food and Drug Administration (FDA) is an agency of the United States Department of Health and Human Services...
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States Supreme Court case to challenge the U.S. Food and Drug Administration (FDA)'s approval of mifepristone, a drug frequently used in medical abortion procedures...
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Montelukast (section FDA investigation)
or after the 2008 FDA communication and prescribing information changes that first publicized the concern. In addition, the FDA's analysis summary of...
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Regulation of tobacco by the U.S. Food and Drug Administration (redirect from FDA Regulation of Tobacco)
the Food and Drug Administration (FDA) was given the ability to regulate tobacco products. Prior to 1996, the FDA played no role in the regulation of...
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FDA v. Wages and White Lion Investments, L.L.C. is a pending United States Supreme Court case about the Food and Drug Administration's denial of approval...
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utmost importance. The FDA can require a pharmaceutical company to place a boxed warning. It is the strongest warning that the FDA requires, and signifies...
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FDA Consumer was a magazine published from 1967 through 2007 by the U.S. Food and Drug Administration (FDA). From 1967 to 1972 it was known as FDA Papers...
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February 2022. "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved...
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Federal Food, Drug, and Cosmetic Act of 1938 (redirect from FDA (510k) filing)
S. Food and Drug Administration (FDA) to oversee the safety of food, drugs, medical devices, and cosmetics. The FDA's principal representative with members...
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Food and Drug Administration (Philippines) (redirect from Food and Drug Administration (FDA Philippines))
The Food and Drug Administration (FDA) of the Philippines, formerly the Bureau of Food and Drugs (BFAD /ˈbiːfæd/; 1982–2009), is a health regulatory agency...
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New Drug Application (redirect from New drug application (FDA))
Administration's (FDA) New Drug Application (NDA) is the vehicle in the United States through which drug sponsors formally propose that the FDA approve a new...
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PrecisionFDA (stylized precisionFDA) is a secure, collaborative, high-performance computing platform that has established a growing community of experts...
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into her" ft. Kirko Bangz - Fame" (2015) "FDA Music: Overgrind". 24Hour HipHop. Retrieved 2015-08-13. "FDA Music feat. Kirko Bangz: 'All Into Her'". AllHipHop...
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Regulation of food and dietary supplements by the U.S. Food and Drug Administration (redirect from FDA regulation of adulterated food)
Drug Administration ("FDA"). Pursuant to the Federal Food, Drug, and Cosmetic Act ("the Act") and accompanying legislation, the FDA has authority to oversee...
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track is a designation by the United States Food and Drug Administration (FDA) of an investigational drug for expedited review to facilitate development...
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August 2020. "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved...
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OpenFDA is a project indexing and formatting Food and Drug Administration (FDA) data, and making it accessible to the public. The ultimate goal of enabling...
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lacking placebo-controlled trials, means that few modern drugs have earned FDA approval as initial monotherapy. In contrast, Europe only requires equivalence...
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FDA preemption is the legal theory in the United States that products licensed or otherwise approved for use by the Food and Drug Administration (FDA)...
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a severe undesired side effect. The U.S. Food and Drug Administration (FDA) has indicated that "it does not appear that the risk [of rhabdomyolysis]...
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Breakthrough therapy (redirect from Breakthrough therapy (FDA))
9 July 2012 Food and Drug Administration Safety and Innovation Act. The FDA's "breakthrough therapy" designation is not intended to imply that a drug...
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August 2020. "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved...
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The United States Food and Drug Administration (FDA) initiated the FDA Accelerated Approval Program in 1992 to allow faster approval of drugs for serious...
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publication produced by the United States Food and Drug Administration (FDA), as required by the Drug Price and Competition Act (Hatch-Waxman Act). The...
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An FDA warning letter is an official message from the United States Food and Drug Administration (FDA) to a manufacturer or other organization that has...
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2009, and had also served as Minister of State for Food & Civil Supplies (FDA) and Labour under Chief Minister Vilasrao Deshmukh between 2004 and 2008...
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