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Journal Abstract Search

513 related items for PubMed ID: 11656783

  • 21. European guidance on medical research.
    Council of Europe. Committee of Ministers.
    Bull Med Ethics; 1990 Mar; No. 56():8-10. PubMed ID: 11650345
    [No Abstract] [Full Text] [Related]

  • 22. The Ethics of Human Experimentation: Reinventing the Research Ethics Board: Proceedings of a National Workshop held in Ottawa, Ontario, March 5-6, 1995.
    National Council on Bioethics in Human Research (Canada).
    NCBHR Commun; 1996 Mar; 7(1):5-35. PubMed ID: 11654527
    [No Abstract] [Full Text] [Related]

  • 23. WHO views on responsibilities of research ethics boards and good clinical practice (GCP).
    Idänpään-Heikkilä J.
    NCBHR Commun; 1993 Mar; 4(2):7-10. PubMed ID: 11652888
    [No Abstract] [Full Text] [Related]

  • 24. The burgeoning law of medical experimentation involving human subjects.
    Bryant LE.
    John Marshall J Pract Proced; 1974 Mar; 8(1):19-51. PubMed ID: 11663465
    [No Abstract] [Full Text] [Related]

  • 25. Medical science, the clinical trial and society.
    Marston RQ.
    Hastings Cent Rep; 1973 Apr; 3(2):1-4. PubMed ID: 11660997
    [No Abstract] [Full Text] [Related]

  • 26. Protection of human subjects.
    United States.
    Code Fed Regul Shipping; 1982 Oct 01; Part 46, Sections 46.101 to 46.306():. PubMed ID: 11660819
    [No Abstract] [Full Text] [Related]

  • 27. The informed-consent policy of the International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use: knowledge is the best medicine.
    Miller MD.
    Cornell Int Law J; 1997 Oct 01; 30(1):203-44. PubMed ID: 11660583
    [No Abstract] [Full Text] [Related]

  • 28. Ethical aspects of pharmaceutically-based clinical investigation: report on a national workshop.
    Miller J, Kinsella D, Klein A, Rusted I.
    NCBHR Commun; 1990 Oct 01; 1(1):7-10. PubMed ID: 11660185
    [No Abstract] [Full Text] [Related]

  • 29. Ethical considerations in European cross-national research.
    Taylor MF.
    Int Soc Sci J; 1994 Dec 01; 46(4):523-32. PubMed ID: 11660701
    [No Abstract] [Full Text] [Related]

  • 30. IRB review of adverse events in investigational drug studies.
    Prentice ED, Gordon B.
    IRB; 1997 Dec 01; 19(6):1-4. PubMed ID: 11656910
    [No Abstract] [Full Text] [Related]

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  • 34. Changing federal regulation of IRBs, Part III: social research and the proposed DHEW regulations.
    Gray BH.
    IRB; 1980 Jan 01; 2(1):1-5+. PubMed ID: 11661793
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