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PUBMED FOR HANDHELDS

Journal Abstract Search

1149 related items for PubMed ID: 19095852

  • 1. The new Food and Drug Administration drug package insert: implications for patient safety and clinical care.
    Watson KT, Barash PG.
    Anesth Analg; 2009 Jan; 108(1):211-8. PubMed ID: 19095852
    [Abstract] [Full Text] [Related]

  • 2. The history and contemporary challenges of the US Food and Drug Administration.
    Borchers AT, Hagie F, Keen CL, Gershwin ME.
    Clin Ther; 2007 Jan; 29(1):1-16. PubMed ID: 17379043
    [Abstract] [Full Text] [Related]

  • 3. Export of pharmaceuticals and medical devices under the federal Food, Drug & Cosmetic Act: FDA's striking change in interpretation post-Shelhigh.
    Basile EM, Tolomeo D, Gluck E.
    Food Drug Law J; 2009 Jan; 64(1):149-69. PubMed ID: 19998744
    [Abstract] [Full Text] [Related]

  • 4. Patient package inserts: the proper prescription?
    Rowe HM.
    Food Drug Law J; 1995 Jan; 50(1):95-124. PubMed ID: 10342988
    [No Abstract] [Full Text] [Related]

  • 5. Prescription drug products; patient package insert requirements--Food and Drug Administration. Final rule.
    Fed Regist; 1981 Jan 02; 46(1):28-30. PubMed ID: 10324121
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  • 7. The FDA announces new prescription drug information format.
    FDA Consum; 2006 Jan 02; 40(2):25-7. PubMed ID: 16671197
    [Abstract] [Full Text] [Related]

  • 8. 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 02; 93(5):981-1002. PubMed ID: 18618967
    [No Abstract] [Full Text] [Related]

  • 9. Vioxx's history and the need for better procedures and better testing.
    Gilhooley M.
    Seton Hall Law Rev; 2007 Jul 02; 37(4):941-68. PubMed ID: 18363218
    [No Abstract] [Full Text] [Related]

  • 10. FDA regulatory compliance reconsidered.
    Tobias C.
    Cornell Law Rev; 2008 Jul 02; 93(5):1003-38. PubMed ID: 18618969
    [No Abstract] [Full Text] [Related]

  • 11. Requirements on content and format of labeling for human prescription drug and biological products. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2006 Jan 24; 71(15):3921-97. PubMed ID: 16479698
    [Abstract] [Full Text] [Related]

  • 12. History of FDA patient package insert requirements.
    Am J Hosp Pharm; 1980 Dec 24; 37(12):1660-1. PubMed ID: 7004180
    [No Abstract] [Full Text] [Related]

  • 13. An overview of the FDA publication Approved Drug Products with Therapeutic Equivalence Evaluations.
    Knoben JE, Scott GR, Tonelli RJ.
    Am J Hosp Pharm; 1990 Dec 24; 47(12):2696-700. PubMed ID: 2278285
    [Abstract] [Full Text] [Related]

  • 14. 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]

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  • 16. Status of certain additional over-the-counter drug category II and III active ingredients. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2002 May 09; 67(90):31123-5. PubMed ID: 12001971
    [Abstract] [Full Text] [Related]

  • 17. Food and Drug Administration requirements for testing and approval of new radiopharmaceuticals.
    Harapanhalli RS.
    Semin Nucl Med; 2010 Sep 09; 40(5):364-84. PubMed ID: 20674596
    [Abstract] [Full Text] [Related]

  • 18. Skin protectant drug products for over-the-counter human use; astringent drug products; final monograph; direct final rule. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Jun 13; 68(114):35290-3. PubMed ID: 12807133
    [Abstract] [Full Text] [Related]

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