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PUBMED FOR HANDHELDS

Journal Abstract Search


336 related items for PubMed ID: 10156421

  • 1. Deterring inefficient pharmaceutical litigation: an economic rationale for the FDA regulatory compliance defense.
    Viscusi WK, Rowland SR, Dorfman HL, Walsh CJ.
    Spec Law Dig Health Care Law; 1996 Mar; (205):9-52. PubMed ID: 10156421
    [No Abstract] [Full Text] [Related]

  • 2. Informed by the European Union experience: what the United States can anticipate and learn from the European Union's regulatory approach to biosimilars.
    Gitter DM.
    Seton Hall Law Rev; 2011 Mar; 41(2):559-92. PubMed ID: 21739759
    [No Abstract] [Full Text] [Related]

  • 3. FDA cracks down on labeling, initiates trial result reporting.
    Osborne R, Waltz E.
    Nat Biotechnol; 2008 Nov; 26(11):1203-4. PubMed ID: 18997742
    [No Abstract] [Full Text] [Related]

  • 4. Pediatric testing of prescription drugs: the Food and Drug Administration's carrot and stick for the pharmaceutical industry.
    Karst KR.
    Am Univ Law Rev; 2000 Nov; 49():739-72. PubMed ID: 11067732
    [No Abstract] [Full Text] [Related]

  • 5. The federal preemption debate in pharmaceutical labeling product liability actions.
    Gross JM, Curry JA.
    Tort Trial Insur Pract Law J; 2007 Nov; 43(1):35-70. PubMed ID: 18354866
    [No Abstract] [Full Text] [Related]

  • 6. US lawmakers tackle safety reforms at the FDA.
    Zwillich T.
    Lancet; 2007 Jun 16; 369(9578):1989-90. PubMed ID: 17577942
    [No Abstract] [Full Text] [Related]

  • 7. Bolstering the FDA's drug-safety authority.
    Schultz WB.
    N Engl J Med; 2007 Nov 29; 357(22):2217-9. PubMed ID: 18046024
    [No Abstract] [Full Text] [Related]

  • 8. Pin the tail on the other donkey: allocating and avoiding injury losses after drug or device approval.
    O'Reilly JT.
    Food Drug Law J; 2007 Nov 29; 62(3):559-72. PubMed ID: 17915397
    [No Abstract] [Full Text] [Related]

  • 9. FDA prohibits extralabel use of two drug classes.
    J Am Vet Med Assoc; 1997 Aug 01; 211(3):269. PubMed ID: 9262656
    [No Abstract] [Full Text] [Related]

  • 10. FDA attempting to overcome major roadblocks in monitoring drug safety.
    Zielinski SL.
    J Natl Cancer Inst; 2005 Jun 15; 97(12):872-3. PubMed ID: 15956645
    [No Abstract] [Full Text] [Related]

  • 11. Accelerated approval of oncology products: the food and drug administration experience.
    Johnson JR, Ning YM, Farrell A, Justice R, Keegan P, Pazdur R.
    J Natl Cancer Inst; 2011 Apr 20; 103(8):636-44. PubMed ID: 21422403
    [Abstract] [Full Text] [Related]

  • 12. PLIVA v. Mensing: generic consumers' unfortunate hand.
    Lee SB.
    Yale J Health Policy Law Ethics; 2012 Apr 20; 12(2):209-63. PubMed ID: 23175916
    [No Abstract] [Full Text] [Related]

  • 13. FDA perspectives on supplement use by patients on antithrombotic therapy: dietary supplement regulatory overview.
    Woo JJ.
    Thromb Res; 2005 Apr 20; 117(1-2):193-6; discussion 201-7. PubMed ID: 16253311
    [No Abstract] [Full Text] [Related]

  • 14. Legal implications of pharmacogenomics regarding drug trials, drug labeling, and genetic testing for drug prescription: an international approach.
    Mandry T.
    Food Drug Law J; 2004 Apr 20; 59(4):519-35. PubMed ID: 15875348
    [Abstract] [Full Text] [Related]

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  • 16. FDA regulatory compliance reconsidered.
    Tobias C.
    Cornell Law Rev; 2008 Jul 20; 93(5):1003-38. PubMed ID: 18618969
    [No Abstract] [Full Text] [Related]

  • 17. Regulatory considerations for determining postmarketing study commitments.
    Meyer RJ.
    Clin Pharmacol Ther; 2007 Aug 20; 82(2):228-30. PubMed ID: 17538552
    [Abstract] [Full Text] [Related]

  • 18. Postmarketing surveillance for oncology drugs.
    Viale PH, Moore S.
    Clin J Oncol Nurs; 2008 Dec 20; 12(6):877-86. PubMed ID: 19064381
    [Abstract] [Full Text] [Related]

  • 19. Prescription for trouble: common drugs, hidden dangers. Tens of people are at risk.
    Consum Rep; 2006 Jan 20; 71(1):34-9. PubMed ID: 16491527
    [No Abstract] [Full Text] [Related]

  • 20. FDA Modernization Act: implications for oncology.
    Morris L.
    Oncology (Williston Park); 1998 Nov 20; 12(11A):139-41. PubMed ID: 10028506
    [Abstract] [Full Text] [Related]


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