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PUBMED FOR HANDHELDS

Journal Abstract Search


104 related items for PubMed ID: 3093882

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  • 4. Over-the-counter human drugs; labeling requirements; final rule; technical amendment. Food and Drug Administration, HHS. Final rule; technical amendment.
    Fed Regist; 2000 Jan 03; 65(1):7-9. PubMed ID: 11010625
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  • 6. Food and Drug Administration--Prescription drug products; patient package inserts requirements. Final rule.
    Fed Regist; 1980 Sep 12; 45(179 Pt 2):60754-84. PubMed ID: 10248285
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  • 7. An interview with FDA Commissioner Frank Young. Interview by Carmella Bocchino.
    Young FE.
    Nurs Econ; 1989 Sep 12; 7(5):242-8. PubMed ID: 2812067
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  • 8. FDA paves the way for drug law reform.
    Eichelberger BM.
    Am J Hosp Pharm; 1978 Jul 12; 35(7):878, 882. PubMed ID: 665706
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  • 9. FDA under attack.
    Mod Vet Pract; 1981 Mar 12; 62(3):197-201. PubMed ID: 7207445
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  • 13. Desperation drugs. Frustrated AIDs patients are spurring the FDA to relax the rules of the game.
    Begley S, Hager M, Wilson L.
    Newsweek; 1989 Aug 07; 114(6):48-9, 51. PubMed ID: 10293942
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  • 14. Investigational new drugs: export requirements for unapproved new drug products. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2005 Nov 23; 70(225):70720-30. PubMed ID: 16304736
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  • 17. Kelsey's Commandos: FDA investigates the investigators.
    Small WE.
    Am Pharm; 1979 Jun 23; 19(6):30-3. PubMed ID: 463736
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  • 19. Development of a course of study in FDA drug regulatory procedures.
    Jacobs RW, King JC.
    Am J Pharm Educ; 1977 May 23; 41(2):185-88. PubMed ID: 10236647
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  • 20. The FDA takes action against unapproved drugs.
    Meadows M.
    FDA Consum; 2007 May 23; 41(1):34-5. PubMed ID: 17342837
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