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PUBMED FOR HANDHELDS

Journal Abstract Search


840 related items for PubMed ID: 17161686

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  • 2. Access before approval--a right to take experimental drugs?
    Okie S.
    N Engl J Med; 2006 Aug 03; 355(5):437-40. PubMed ID: 16885545
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  • 11. The Food and Drug Administration's use of postmarketing (Phase IV) study requirements: exception to the rule?
    Steenburg C.
    Food Drug Law J; 2006 Aug 03; 61(2):295-383. PubMed ID: 16903034
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  • 12. Despite criticism of the FDA review process, new cancer drugs reach patients sooner in the United States than in Europe.
    Roberts SA, Allen JD, Sigal EV.
    Health Aff (Millwood); 2011 Jul 03; 30(7):1375-81. PubMed ID: 21680577
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  • 15. The Prescription Drug User Fee Act: is a faster Food and Drug Administration always a better Food and Drug Administration?
    Zelenay JL.
    Food Drug Law J; 2005 Jul 03; 60(2):261-338. PubMed ID: 16094773
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  • 16. Shifting terrain in the regulation of off-label promotion of pharmaceuticals.
    Mello MM, Studdert DM, Brennan TA.
    N Engl J Med; 2009 Apr 09; 360(15):1557-66. PubMed ID: 19357413
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  • 17. Changing requirements for evaluation of pharmacologic agents.
    Chesney RW, Christensen ML.
    Pediatrics; 2004 Apr 09; 113(4 Suppl):1128-32. PubMed ID: 15060209
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  • 18. Biopharmaceutical statistics in a pharmaceutical regulated environment: past, present, and future.
    Segreti AC, Leung HM, Koch GG, Davis RL, Mohberg NR, Peace KE.
    J Biopharm Stat; 2001 Nov 09; 11(4):347-72. PubMed ID: 12018784
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