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Journal Abstract Search

345 related items for PubMed ID: 15698532

  • 1. Optimising the design of preliminary toxicity studies for pharmaceutical safety testing in the dog.
    Smith D, Combes R, Depelchin O, Jacobsen SD, Hack R, Luft J, Lammens L, von Landenberg F, Phillips B, Pfister R, Rabemampianina Y, Sparrow S, Stark C, Stephan-Gueldner M.
    Regul Toxicol Pharmacol; 2005 Mar; 41(2):95-101. PubMed ID: 15698532
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  • 2. Use of the dog as non-rodent test species in the safety testing schedule associated with the registration of crop and plant protection products (pesticides): present status.
    Box RJ, Spielmann H.
    Arch Toxicol; 2005 Nov; 79(11):615-26. PubMed ID: 15940470
    [Abstract] [Full Text] [Related]

  • 3. Working in partnership to advance the 3Rs in toxicity testing.
    Holmes AM, Creton S, Chapman K.
    Toxicology; 2010 Jan 12; 267(1-3):14-9. PubMed ID: 19903508
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  • 4. What have we learned from pre-clinical juvenile toxicity studies?
    Bailey GP, Mariën D.
    Reprod Toxicol; 2009 Sep 12; 28(2):226-9. PubMed ID: 19446432
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  • 5. [Replacement of dogs as research animals for the approval testing of plant protection products].
    Box RJ.
    ALTEX; 2006 Sep 12; 23(1):24-7. PubMed ID: 16477345
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  • 6. Real life juvenile toxicity case studies: the good, the bad and the ugly.
    De Schaepdrijver L, Rouan MC, Raoof A, Bailey GP, De Zwart L, Monbaliu J, Coogan TP, Lammens L, Coussement W.
    Reprod Toxicol; 2008 Sep 12; 26(1):54-5. PubMed ID: 18514481
    [Abstract] [Full Text] [Related]

  • 7. High dose selection in general toxicity studies for drug development: A pharmaceutical industry perspective.
    Buckley LA, Dorato MA.
    Regul Toxicol Pharmacol; 2009 Aug 12; 54(3):301-7. PubMed ID: 19477212
    [Abstract] [Full Text] [Related]

  • 8. Juvenile animal toxicity study designs to support pediatric drug development.
    Cappon GD, Bailey GP, Buschmann J, Feuston MH, Fisher JE, Hew KW, Hoberman AM, Ooshima Y, Stump DG, Hurtt ME.
    Birth Defects Res B Dev Reprod Toxicol; 2009 Dec 12; 86(6):463-9. PubMed ID: 20025047
    [Abstract] [Full Text] [Related]

  • 9. Safety and nutritional assessment of GM plants and derived food and feed: the role of animal feeding trials.
    EFSA GMO Panel Working Group on Animal Feeding Trials.
    Food Chem Toxicol; 2008 Mar 12; 46 Suppl 1():S2-70. PubMed ID: 18328408
    [Abstract] [Full Text] [Related]

  • 10. The timing of preclinical toxicological studies: pharmaceutical company approaches to toxicity testing in support of initial clinical investigations.
    Parkinson C, Thomas KE, Lumley CE.
    Regul Toxicol Pharmacol; 1996 Apr 12; 23(2):162-72. PubMed ID: 8661335
    [Abstract] [Full Text] [Related]

  • 11. Review of the performance of the 3T3 NRU in vitro phototoxicity assay in the pharmaceutical industry.
    Lynch AM, Wilcox P.
    Exp Toxicol Pathol; 2011 Mar 12; 63(3):209-14. PubMed ID: 20060695
    [Abstract] [Full Text] [Related]

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  • 13. Safety evaluation to support First-In-Man investigations II: toxicology studies.
    Baldrick P.
    Regul Toxicol Pharmacol; 2008 Jul 12; 51(2):237-43. PubMed ID: 18501490
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  • 15. Embryo-fetal developmental toxicity study design for pharmaceuticals.
    Wise LD, Buschmann J, Feuston MH, Fisher JE, Hew KW, Hoberman AM, Lerman SA, Ooshima Y, Stump DG.
    Birth Defects Res B Dev Reprod Toxicol; 2009 Dec 12; 86(6):418-28. PubMed ID: 20025038
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