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  2. United States v. Park - Wikipedia

    en.wikipedia.org/wiki/United_States_v._Park

    Sections 402 and 301 of the Act prohibited adulterating food held for sale in interstate commerce. [2] Park was the CEO of Acme Markets, Inc. [3] In 1971, the FDA notified Acme and Park that a 12-day inspection revealed insanitary conditions and vermin contamination. [4]

  3. Biologics license application - Wikipedia

    en.wikipedia.org/wiki/Biologics_License_Application

    A biologics license application (BLA) is defined by the U.S. Food and Drug Administration (FDA) as follows: The biologics license application is a request for permission to introduce, or deliver for introduction, a biologic product into interstate commerce (21 CFR 601.2). The BLA is regulated under 21 CFR 600 – 680.

  4. Food and Drug Administration (Philippines) - Wikipedia

    en.wikipedia.org/wiki/Food_and_Drug...

    The Food and Drug Administration (FDA) of the Philippines, formerly the Bureau of Food and Drugs (BFAD / ˈ b iː f æ d /; 1982–2009), is a health regulatory agency under the Department of Health created on 1963 by Republic Act No. 3720, amended on 1987 by Executive Order 175 otherwise known as the "Food, Drugs and Devices, and Cosmetics Act", and subsequently reorganized by Republic Act No ...

  5. Independent agencies of the United States government

    en.wikipedia.org/wiki/Independent_agencies_of...

    The Interstate Commerce Commission regulated common carriers and was thus able to render far reaching orders, such as the desegregation of public transportation. After trucking and railroads were largely deregulated, the ICC was replaced with the independent Surface Transportation Board , with remaining functions transferred to the Department ...

  6. Food and Drug Administration - Wikipedia

    en.wikipedia.org/wiki/Food_and_Drug_Administration

    The United States 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 and promoting public health through the control and supervision of food safety, tobacco products, caffeine products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines ...

  7. Center for Biologics Evaluation and Research - Wikipedia

    en.wikipedia.org/wiki/Center_for_Biologics...

    As of July 2006 CBER's authority resides in sections 351 and 361 of the Public Health Service Act and in various sections of the Food, Drug and Cosmetic Act. [3]Section 351 of the Public Health Service Act requires licensure of biological products that travel in interstate commerce in the United States.

  8. US FTC sues drug 'gatekeepers' over high insulin prices - AOL

    www.aol.com/news/us-ftc-sues-drug-gatekeepers...

    The case accuses UnitedHealth Group Inc's Optum unit, CVS Health Corp's CVS Caremark and Cigna Corp's Express Scripts of unfairly excluding lower cost insulin products from lists of drugs covered ...

  9. Fair Packaging and Labeling Act - Wikipedia

    en.wikipedia.org/wiki/Fair_Packaging_and...

    To regulate interstate and foreign commerce by preventing the use of unfair or deceptive methods of packaging or labeling of certain consumer commodities distributed in such commerce, and for other purposes. Acronyms (colloquial) FPLA: Enacted by: the 89th United States Congress: Effective: November 3, 1966: Citations; Public law: 89-755 ...