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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

479 related items for PubMed ID: 18046024

  • 41. What ails the FDA?
    Okie S.
    N Engl J Med; 2005 Mar 17; 352(11):1063-6. PubMed ID: 15784660
    [No Abstract] [Full Text] [Related]

  • 42. FDA tightens its grip on drug regulation.
    Coombes R.
    BMJ; 2007 Feb 10; 334(7588):290-1. PubMed ID: 17289729
    [Abstract] [Full Text] [Related]

  • 43. Permitting product liability litigation for FDA-approved drugs and devices promotes patient safety.
    Kesselheim AS.
    Clin Pharmacol Ther; 2010 Jun 10; 87(6):645-7. PubMed ID: 20485322
    [Abstract] [Full Text] [Related]

  • 44. Pharmaceuticals and medical devices: FDA oversight. Issue brief.
    Berry MD.
    Issue Brief Health Policy Track Serv; 2012 Dec 31; ():1-79. PubMed ID: 23297449
    [No Abstract] [Full Text] [Related]

  • 45. Science and regulation. FDA's approach to regulation of products of nanotechnology.
    Hamburg MA.
    Science; 2012 Apr 20; 336(6079):299-300. PubMed ID: 22517845
    [No Abstract] [Full Text] [Related]

  • 46. The impact of FDA reform.
    Trunzo J.
    Med Device Technol; 2003 Apr 20; 14(3):36-7. PubMed ID: 12789699
    [Abstract] [Full Text] [Related]

  • 47. Does $760 m a year of industry funding affect the FDA's drug approval process?
    Wolfe SM.
    BMJ; 2014 Aug 05; 349():g5012. PubMed ID: 25096994
    [No Abstract] [Full Text] [Related]

  • 48. The FDA and deference lost: a self-inflicted wound or the product of a wounded agency? A response to Professor O'Reilly.
    Vladeck DC.
    Cornell Law Rev; 2008 Jul 05; 93(5):981-1002. PubMed ID: 18618967
    [No Abstract] [Full Text] [Related]

  • 49. Antiperspirant drug products for over-the-counter human use; final monograph. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Jun 09; 68(110):34273-93. PubMed ID: 12795305
    [Abstract] [Full Text] [Related]

  • 50. Good law from tragic facts--Congress, the FDA, and preemption.
    Annas GJ.
    N Engl J Med; 2009 Sep 17; 361(12):1206-11. PubMed ID: 19759383
    [No Abstract] [Full Text] [Related]

  • 51. Applications for Food and Drug Administration application approval to market a new drug; revision of postmarketing reporting requirements. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2007 Oct 18; 72(201):58993-9000. PubMed ID: 17966558
    [Abstract] [Full Text] [Related]

  • 52. Drug safety: a contrarian's point of view.
    Cobert B.
    Food Drug Law J; 2007 Oct 18; 62(3):501-12. PubMed ID: 17915392
    [No Abstract] [Full Text] [Related]

  • 53. "Safer, but not safe enough".
    Crombie HD.
    Conn Med; 2006 Oct 18; 70(10):645. PubMed ID: 17190395
    [No Abstract] [Full Text] [Related]

  • 54. Off-label or off-limits?
    Ratner M, Gura T.
    Nat Biotechnol; 2008 Aug 18; 26(8):867-75. PubMed ID: 18688236
    [No Abstract] [Full Text] [Related]

  • 55. Pediatric research: coming of age in the new millennium.
    Milne CP.
    Am J Ther; 1999 Sep 18; 6(5):263-82. PubMed ID: 11329108
    [Abstract] [Full Text] [Related]

  • 56. FDA drug labeling for pregnancy and lactation drug safety monitoring systems.
    Greene MF.
    Semin Perinatol; 2015 Nov 18; 39(7):520-3. PubMed ID: 26428020
    [Abstract] [Full Text] [Related]

  • 57. Red sky in the morning: modifying prescription drug labels as a result of postmarket surveillance.
    Jacobson JD, Feigal D.
    Food Drug Law J; 2007 Nov 18; 62(3):529-46. PubMed ID: 17915395
    [No Abstract] [Full Text] [Related]

  • 58. The challenges of globalization in pharmaceutical law--is an international drug approval system modeled after the European system worth considering?
    Purnhagen KP.
    Food Drug Law J; 2008 Nov 18; 63(3):623-45. PubMed ID: 19031663
    [No Abstract] [Full Text] [Related]

  • 59.
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