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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

124 related items for PubMed ID: 1517124

  • 21. Developing data to satisfy drug and pesticide approval requirements of FDA, EPA, and USDA; are cattle, sheep, and poultry minor species?
    Gessert RA.
    Proc Annu Meet U S Anim Health Assoc; 1975; (79):262-5. PubMed ID: 1078055
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  • 22. To live or not to live with the risk of extra-label use.
    Herrick JB.
    J Am Vet Med Assoc; 1992 Jun 15; 200(12):1827. PubMed ID: 1639684
    [No Abstract] [Full Text] [Related]

  • 23. The reformation of animal drug law: the impact of 1996.
    Lambert EI.
    Food Drug Law J; 1997 Jun 15; 52(3):277-89. PubMed ID: 10343026
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  • 27. Developments in food and drug law.
    Masoudi GF.
    Food Drug Law J; 2005 Jun 15; 60(2):107-16. PubMed ID: 16097088
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  • 32. FDA's role in drug product recalls.
    Crawford SY.
    Am J Hosp Pharm; 1991 Dec 15; 48(12):2595-6. PubMed ID: 1814194
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  • 33. FDA's treatment investigational new drug rule: one year later.
    Appler WD.
    J Clin Psychopharmacol; 1988 Aug 15; 8(4):286-7. PubMed ID: 3209720
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  • 34. Current food safety and quality service residue control program.
    Engel RE.
    J Am Vet Med Assoc; 1980 May 15; 176(10 Spec No):1145-7. PubMed ID: 7216889
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  • 35. FDA tightens screws on extra-label drug use, liberalizes policy on use of human drugs in animals.
    Gloyd JS.
    J Am Vet Med Assoc; 1992 Sep 01; 201(5):676-7. PubMed ID: 1399765
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  • 36. DSHEA provisions confine FDA's authority to issue regulations that concern allegedly adulterated dietary supplements.
    McNamara SH, Siegner AW, Phelps EP.
    Food Drug Law J; 1999 Sep 01; 54(4):595-8. PubMed ID: 11824456
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