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  2. Approved Drug Products with Therapeutic Equivalence ...

    en.wikipedia.org/wiki/Approved_Drug_Products...

    Approved Drug Products with Therapeutic Equivalence Evaluations, commonly known as the Orange Book, is a publication produced by the United States Food and Drug Administration (FDA), as required by the Drug Price and Competition Act (Hatch-Waxman Act). The Hatch-Waxman Act was created to '"strike a balance between two competing policy interests:

  3. Center for Food Safety and Applied Nutrition - Wikipedia

    en.wikipedia.org/wiki/Center_for_Food_Safety_and...

    The Center for Food Safety and Applied Nutrition (CFSAN (/ ˈ s ɪ f ˌ s æ n / SIF-san)) is the branch of the United States Food and Drug Administration (FDA) that regulates food, dietary supplements, and cosmetics, as opposed to drugs, biologics, medical devices, and radiological products, which also fall under the purview of the FDA.

  4. List of federal installations in Maryland - Wikipedia

    en.wikipedia.org/wiki/List_of_federal...

    Food and Drug Administration (FDA) White Oak: Intelligence Advanced Research Projects Activity (IARPA) Bethesda: Intelligence Community Campus-Bethesda (ICC-B) Bethesda: Internal Revenue Service (IRS) New Carrollton: National Archives and Records Administration (NARA) College Park: NASA's Goddard Space Flight Center: Greenbelt: Naval Air ...

  5. List of OMB Circulars and Bulletins - Wikipedia

    en.wikipedia.org/wiki/List_of_OMB_Circulars_and...

    Circular A-131: Value Engineering, issued 26 January 1988, revised 21 May 1993 [2] and 26 December 2013. Contains guidance to support the sustained use of value engineering by federal departments and agencies; Circular A-133: Audits of states, local government and non-profit organizations: see OMB A-133 Compliance Supplement

  6. DailyMed - Wikipedia

    en.wikipedia.org/wiki/DailyMed

    DailyMed is a website operated by the U.S. National Library of Medicine (NLM) to publish up-to-date and accurate drug labels (also called a "package insert") to health care providers and the general public. The contents of DailyMed is provided and updated daily by the U.S. Food and Drug Administration (FDA). The FDA in turn collects this ...

  7. Ban on caffeinated alcoholic drinks in the United States

    en.wikipedia.org/wiki/Ban_on_caffeinated...

    On November 17, 2010, the United States FDA introduced a ban on caffeinated alcoholic drinks, preventing the marketing and distribution of any prepackaged caffeinated alcoholic drink. [1] Such a ban was discussed as a result of multiple cases of alcohol poisoning and alcohol-related blackouts among users of such drinks. The majority of these ...

  8. Office of Global Regulatory Operations and Policy - Wikipedia

    en.wikipedia.org/wiki/Office_of_Global...

    FDA Building 32 houses the Office of the Commissioner and the Office of Regulatory Affairs. The Office of Global Regulatory Operations and Policy (GO), [1] also known as the Office of Regulatory Affairs (ORA), [2] is the part of the U.S. Food and Drug Administration (FDA) enforcing the federal laws governing biologics, cosmetics, dietary supplements, drugs, food, medical devices, radiation ...

  9. Center for Biologics Evaluation and Research - Wikipedia

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

    Originally, CBER was part of what became the National Institutes of Health, rather than the FDA. [8] Its mission included a mandate to foster the development of new vaccines. [8] The Bureau was transferred from the NIH to the FDA in 1972, where it was renamed Bureau of Biologics and focused on vaccines, serums for allergy shots, and blood ...