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PUBMED FOR HANDHELDS

Journal Abstract Search


540 related items for PubMed ID: 11993366

  • 1. A critical tipping point.
    Zuckerman MB.
    US News World Rep; 2002 Apr 22; 132(13):72. PubMed ID: 11993366
    [No Abstract] [Full Text] [Related]

  • 2. The FDA's drug review process: ensuring drugs are safe and effective.
    Meadows M.
    FDA Consum; 2002 Apr 22; 36(4):19-24. PubMed ID: 12184298
    [No Abstract] [Full Text] [Related]

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  • 6. FDA and EMEA pool scientific advice.
    Katsnelson A.
    Nat Biotechnol; 2004 Dec 22; 22(12):1490-1. PubMed ID: 15583642
    [No Abstract] [Full Text] [Related]

  • 7. Balancing US patent and FDA approval processes: strategically optimizing market exclusivity.
    Fernandez DS, Huie JT.
    Drug Discov Today; 2004 Jun 15; 9(12):509-12. PubMed ID: 15183155
    [No Abstract] [Full Text] [Related]

  • 8. The big gap at the FDA.
    Stipp D.
    Fortune; 2002 Jul 22; 146(2):113-4, 116. PubMed ID: 12141178
    [No Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Drugs with breakthrough status charm investors.
    Senior M.
    Nat Biotechnol; 2013 Nov 17; 31(11):945-7. PubMed ID: 24213748
    [No Abstract] [Full Text] [Related]

  • 11. The Prescription Drug User Fee Act of 1992: speeding up the drug approval process.
    Bierut MB.
    Healthspan; 1992 Dec 17; 9(11):12-4. PubMed ID: 10123552
    [No Abstract] [Full Text] [Related]

  • 12. BIO and biogenerics.
    Feldbaum CB.
    Nat Biotechnol; 2005 Jan 17; 23(1):17; discussion 17. PubMed ID: 15637607
    [No Abstract] [Full Text] [Related]

  • 13. Trials and error.
    Jacobs T.
    Nat Biotechnol; 2005 Dec 17; 23(12):1481. PubMed ID: 16333284
    [No Abstract] [Full Text] [Related]

  • 14. The special treatment.
    Osborne R.
    Nat Biotechnol; 2008 May 17; 26(5):487-9. PubMed ID: 18464770
    [No Abstract] [Full Text] [Related]

  • 15. Steve Carney talks to Vincent Lee on the pharma industry, the FDA and public education with respect to drugs and their development.
    Lee VH.
    Drug Discov Today; 2005 Nov 01; 10(21):1411-4. PubMed ID: 16243258
    [No Abstract] [Full Text] [Related]

  • 16. The drive to reform the FDA gains momentum.
    Gatty B.
    Hosp Formul; 1995 Mar 01; 30(3):178, 177. PubMed ID: 10141250
    [No Abstract] [Full Text] [Related]

  • 17. Maine law requires drug companies to provide clinical trial data.
    Appell D.
    J Natl Cancer Inst; 2005 Sep 07; 97(17):1246. PubMed ID: 16145043
    [No Abstract] [Full Text] [Related]

  • 18. 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 Sep 07; 60(2):261-338. PubMed ID: 16094773
    [No Abstract] [Full Text] [Related]

  • 19. Drive for drugs leads to baby clinical trials.
    Nature; 2006 Mar 23; 440(7083):406-7. PubMed ID: 16554774
    [No Abstract] [Full Text] [Related]

  • 20. Who would approve new drugs if there were no FDA?
    Gatty B.
    Hosp Formul; 1995 Jan 23; 30(1):58, 57. PubMed ID: 10139726
    [No Abstract] [Full Text] [Related]


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