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Journal Abstract Search


1456 related items for PubMed ID: 15239181

  • 1. Informed consent in clinical research: policies and practices in Singapore.
    Ramachandran AJ.
    J Biolaw Bus; 2003; 6(1):65-75. PubMed ID: 15239181
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  • 3. [Clinical trials in developing countries: who should define ethics?].
    Béréterbide F, Hirsch F.
    Bull Soc Pathol Exot; 2008 Apr; 101(2):102-5. PubMed ID: 18543701
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  • 4. The basics of human subjects protection.
    Yoder LH.
    Medsurg Nurs; 2006 Apr; 15(2):95-8; quiz 99. PubMed ID: 16700248
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  • 7. Research involving children: regulations, review boards and reform.
    Gandhi R.
    J Health Care Law Policy; 2005 Apr; 8(2):264-330. PubMed ID: 16471026
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  • 8. Pragmatism as a complementary approach to legislation: closing regulatory gaps in human subject research.
    Vernillo A.
    Am J Bioeth; 2008 Nov; 8(11):15-7. PubMed ID: 19061099
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  • 12. Excluding particular information from consent forms.
    Dickert N, Kass N, Paasche-Orlow M, Taylor H.
    Account Res; 2005 Nov; 12(1):33-45. PubMed ID: 16021790
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  • 15. Research column: protection of children as subjects in research.
    Nelson AE.
    J Pediatr Oncol Nurs; 2003 Nov; 20(3):141-3. PubMed ID: 12776262
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  • 17. European Union clinical trials directive.
    Bull Med Ethics; 2001 Jul; (169):13-24. PubMed ID: 11878337
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  • 18. Informed consent: between ethics and law.
    Pilotto F, Badon P.
    Dolentium Hominum; 2002 Jul; 17(3):29-34. PubMed ID: 16459395
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  • 19. The role of institutional review boards in protecting human subjects: are we really ready to fix a broken system?
    Beh HG.
    Law Psychol Rev; 2002 Jul; 26(1):1-47. PubMed ID: 16514756
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  • 20. Ethical oversight of research in developing countries.
    Kass N, Dawson L, Loyo-Berrios NI.
    IRB; 2003 Jul; 25(2):1-10. PubMed ID: 12833901
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