About: Federal Food, Drug, and Cosmetic Act

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The United States Federal Food, Drug, and Cosmetic Act (abbreviated as FFDCA, FDCA, or FD&C) is a set of laws passed by the United States Congress in 1938 giving authority to the U.S. Food and Drug Administration (FDA) to oversee the safety of food, drugs, medical devices, and cosmetics. A principal author of this law was Royal S. Copeland, a three-term U.S. senator from New York. In 1968, the Electronic Product Radiation Control provisions were added to the FD&C. Also in that year the FDA formed the Drug Efficacy Study Implementation (DESI) to incorporate into FD&C regulations the recommendations from a National Academy of Sciences investigation of effectiveness of previously marketed drugs. The act has been amended many times, most recently to add requirements about bioterrorism preparat

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rdf:type	Thing
rdfs:label	Federal Food, Drug, and Cosmetic Act (en) قانون الغذاء والدواء ومواد التجميل (ar) Federal Food, Drug, and Cosmetic Act (de) Ley Federal de Alimentos, Medicamentos y Cosméticos de Estados Unidos (es) Federal Food, Drug and Cosmetic Act (fr) 連邦食品・医薬品・化粧品法 (ja) Federalna ustawa o żywności, lekach i kosmetykach (pl) Lei Federal de Alimentos, Medicamentos e Cosméticos dos Estados Unidos (pt) 联邦食品、药品和化妆品法案 (zh)
rdfs:comment	Le Federal Food, Drug and Cosmetic Act est une loi fédérale américaine, signée en 1938 par le président Roosevelt, à la suite du scandale de l'année précédente lors duquel une centaine de personnes étaient décédées à la suite de l'ingestion de l'élixir sulfanilamide, médicament rendu toxique par la présence de diéthylène glycol. Venant après le Pure Food and Drug Act de 1906, qui mènera à la création de la Food and Drug Administration (FDA), cette nouvelle loi vient renforcer les pouvoirs de l'administration fédérale et en particulier de la FDA en matière d'autorisation de mise sur le marché (AMM) des médicaments et produits cosmétiques. (fr) 連邦食品・医薬品・化粧品法（れんぽうしょくひんいやくひんけしょうひんほう、英語: Federal Food, Drug, and Cosmetic Act、略称: FFDCA、FDCA、FD&C）は、アメリカ食品医薬品局（FDA）に、食の安全性、薬品、化粧品に関する権限を与える法律である。1938年にアメリカ合衆国議会で可決された。この法律の主な著者はニューヨークから上院議員に三選したRoyal S. Copelandである。1968年には、電子製品からの放射線の管理条項が追加された。またこの年にFDAは、米国科学アカデミーによるFD&C法以前の市販医薬品の有効性についての勧告を組み込むために（DESI）を作成した。この法律は何度も改正されており、最近ではバイオテロに関する条項の準備が要求されている。 (ja) Federalna ustawa o żywności, lekach i kosmetykach (ang. Federal Food, Drug, and Cosmetic Act, FFDCA, FDCA, FD&C) – akt prawny uchwalony przez Kongres Stanów Zjednoczonych w 1938 roku, dający Agencji Żywności i Leków prawo nadzorowania bezpieczeństwa żywności, leków i kosmetyków. (pl) Lei Federal de Alimentos, Medicamentos e Cosméticos dos Estados Unidos (em inglês The United States Federal Food, Drug, and Cosmetic Act abreviado como FFDCA, FDCA ou FD&C), é um conjunto de lei aprovadas pelo Congresso em 1938, que deu autoridade à Food and Drug Administration (FDA) para supervisionar a segurança dos alimentos, medicamentos e cosméticos. O autor principal desta lei foi , que foi senador pelo estado de Nova York por três mandatos. (pt) 美国联邦食品、药品和化妆品法案（常缩写为FFDCA，FDCA，或FD&C）是美国国会在1938年通过的一系列法案的总称，赋予美国食品药品监督管理局（FDA）监督监管食品安全、药品、及化妆品的权力。该法案主要是由写成，其为一三年期的纽约州参议员。该法案通过后又历经多次修改。催生该法案的主要原因之一是因为一种磺胺药物中所使用的溶剂二甘醇导致100多名病人死亡。这部法案诞生后取代了1906年通过的。 (zh) القانون الفدرالي الأمريكي للغذاء والدواء ومواد التجميل Federal Food, Drug, and Cosmetic Act ، واختصاره (FFDCA أو FDCA أو FD & C) وهو مجموعة من القوانين التي أقرها الكونغرس في عام 1938 ويعطي سلطة لإدارة الغذاء والدواء الأمريكية (FDA) للإشراف على سلامة الغذاء والأدوية، ومستحضرات التجميل. (ar) Der Federal Food, Drug, and Cosmetic Act (abgekürzt FFDCA, FDCA oder FD&C) umfasst eine Reihe gesetzlicher Regelungen, die die Food and Drug Administration dazu ermächtigen, die Sicherheit von Lebensmitteln, Arzneimitteln, medizinischen Produkten und Kosmetik zu überwachen und wurde 1938 vom US-Kongress verabschiedet. Hauptautor des Gesetzes war Royal S. Copeland, ein Senator aus New York. 1968 wurden Bestimmungen zur Kontrolle der Strahlung elektronischer Produkte in den FD&C Act aufgenommen. Das Gesetz wurde bereits mehrfach geändert. (de) The United States Federal Food, Drug, and Cosmetic Act (abbreviated as FFDCA, FDCA, or FD&C) is a set of laws passed by the United States Congress in 1938 giving authority to the U.S. Food and Drug Administration (FDA) to oversee the safety of food, drugs, medical devices, and cosmetics. A principal author of this law was Royal S. Copeland, a three-term U.S. senator from New York. In 1968, the Electronic Product Radiation Control provisions were added to the FD&C. Also in that year the FDA formed the Drug Efficacy Study Implementation (DESI) to incorporate into FD&C regulations the recommendations from a National Academy of Sciences investigation of effectiveness of previously marketed drugs. The act has been amended many times, most recently to add requirements about bioterrorism preparat (en) La Ley Federal de Alimentos, Medicamentos y Cosméticos de Estados Unidos (en inglés, The United States Federal Food, Drug, and Cosmetic Act, abreviada como FFDCA, FDCA o FD & C) es un conjunto de leyes aprobadas por el Congreso de los Estados Unidos en 1938, que dio autoridad a la Agencia de Medicamentos y Alimentación (Food and Drug Administration, FDA) para supervisar la seguridad de los alimentos, medicamentos y cosméticos. El autor principal de esta ley fue , quien fue senador por el estado de Nueva York durante tres legislaturas. En 1968, se agregaron ciertas disposiciones sobre el control de la radiación de los productos electrónicos. También en ese año la FDA creó el Drug Efficacy Study Implementation —DESI— (Implementación del Estudio de la Eficacia de los Medicamentos) para incor (es)
dcterms:subject	75th United States Congress Food safety in the United States 1938 in American law Pharmaceuticals policy United States federal health legislation Drug policy of the United States Food and Drug Administration Food law
Wikipage page ID	1271173 (xsd:integer)
Wikipage revision ID	1124306603 (xsd:integer)
Link from a Wikipage to another Wikipage	Prescription Drug User Fee Act Public Health Service Act Pure Food and Drug Act Royal S. Copeland List of food additives Mineral water New Drug Application Regulation of therapeutic goods Animal Medicinal Drug Use Clarification Act Trademark Act of 1946 75th United States Congress Biologics Control Act Bottled water Democratic Party (United States) Homeopathy United States Congress United States House of Representatives United States v. Park Strict liability 100,000,000 Guinea Pigs Food safety in the United States Commerce clause Controlled Substances Act Cosmetics Criminal law Medical Device Regulation Act Safe Medical Device Amendments of 1990 Chewing gum Elixir sulfanilamide Office of Criminal Investigations Citrus Red 2 Electroconvulsive therapy Franklin D. Roosevelt Government in the Sunshine Act Legal Information Institute Mammography Quality Standards Act Clinical trial Dental floss Federal Advisory Committee Act Brilliant blue FCF 1938 in American law Drug Drug Efficacy Study Implementation Drugs in the United States Title 21 of the United States Code 21st Century Cures Act Pharmaceuticals policy Allura Red AC Amalgam (dentistry) United States federal health legislation Durham-Humphrey Amendment Erythrosine Fair Packaging and Labeling Act Fast Green FCF Federal Meat Inspection Act Federal Trade Commission Food Quality Protection Act Food and Drug Administration Food and Drug Administration Amendments Act of 2007 Food and Drug Administration Revitalization Act Food supplement Center for Food Safety and Applied Nutrition Diana Zuckerman Dietary supplement Food additive Food and Drug Administration Modernization Act of 1997 Food coloring Food safety Medical device United States Government Publishing Office Private law

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