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PUBMED FOR HANDHELDS

Journal Abstract Search


306 related items for PubMed ID: 19999637

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  • 22. Enforcement related to off-label marketing and use of drugs and devices: where have we been and where are we going?
    Joseph JN, Deaton D, Ehsan H, Bonanno MA.
    J Health Life Sci Law; 2009 Jan; 2(2):73-108. PubMed ID: 19288889
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  • 24. Dissemination of information on unapproved/new uses for marketed drugs, biologics, and devices--FDA. Proposed rule.
    Fed Regist; 1998 Jun 08; 63(109):31143-61. PubMed ID: 10180130
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  • 33. Disqualification of a clinical investigator--FDA. Final rule.
    Fed Regist; 1997 Sep 05; 62(172):46875-6. PubMed ID: 10173286
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  • 34. FDA Modernization Act: implications for oncology.
    Morris L.
    Oncology (Williston Park); 1998 Nov 05; 12(11A):139-41. PubMed ID: 10028506
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  • 35. Prescribing medications in pediatrics: concerns regarding FDA approval and pharmacokinetics.
    Novak E, Allen PJ.
    Pediatr Nurs; 2007 Nov 05; 33(1):64-70. PubMed ID: 17411005
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  • 37. Inconsistent government policies: why FDA off-label regulation cannot survive First Amendment review under Greater New Orleans.
    Hall RF, Sobotka E.
    Food Drug Law J; 2007 Nov 05; 62(1):1-48. PubMed ID: 17444025
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  • 38. Unapproved uses of approved drugs: the physician, the package insert, and the Food and Drug Administration: subject review. American Academy of Pediatrics Committee on Drugs.
    Pediatrics; 1996 Jul 05; 98(1):143-5. PubMed ID: 8668390
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  • 39. 'Off-label' drug use: an FDA regulatory term, not a negative implication of its medical use.
    Meadows WA, Hollowell BD.
    Int J Impot Res; 2008 Jul 05; 20(2):135-44. PubMed ID: 18004389
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  • 40. Risk management and intrusions on medical practice: striking a balance.
    Enzi MB, Kennedy EM.
    Health Aff (Millwood); 2007 Jul 05; 26(3):678-80. PubMed ID: 17485743
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