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PUBMED FOR HANDHELDS

Journal Abstract Search


344 related items for PubMed ID: 11659358

  • 21. Mapping the human genome.
    Grisolia S.
    Hastings Cent Rep; 1989; 19(4):S18-9. PubMed ID: 11650225
    [Abstract] [Full Text] [Related]

  • 22. Proposed requirements for informed consent go beyond current federal regulations.
    Hum Res Rep; 1994 Jul; 9(7):1-3. PubMed ID: 11659879
    [No Abstract] [Full Text] [Related]

  • 23. U.S. Bioethics Commission meets, outlines agenda.
    Fox JL.
    Nat Biotechnol; 1996 Nov; 14(11):1533. PubMed ID: 11644890
    [No Abstract] [Full Text] [Related]

  • 24. Much more research to fall under IRB review.
    Maloney DM.
    Hum Res Rep; 1999 Jul; 14(7):3. PubMed ID: 11658059
    [No Abstract] [Full Text] [Related]

  • 25. Health Research Extension Act of 1985. Public Law 99-158.
    United States.
    US Statut Large; 1985 Jul; 99(Title IV Sections 1-12):. PubMed ID: 11686169
    [No Abstract] [Full Text] [Related]

  • 26. Symposium on the Law of 20 December 1988 Concerning Biomedical Research on Human Subjects: Protection Committee or Ethics Committee?
    J Int Bioethique; 1993 Mar; 4(Special Issue):61-4. PubMed ID: 11652137
    [No Abstract] [Full Text] [Related]

  • 27. International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) adopts Consolidated Guideline on Good Clinical Practice in the Conduct of Clinical Trials on Medicinal Products for Human Use.
    Int Dig Health Legis; 1997 Mar; 48(2):231-4. PubMed ID: 11656783
    [No Abstract] [Full Text] [Related]

  • 28. The Human Genome Project: bibliography of ethical, social, legal, and scientific aspects.
    Arizona State University Center for the Study of Law, Science and Technology.
    Jurimetrics; 1992 Mar; 32(2):223-311. PubMed ID: 11659418
    [No Abstract] [Full Text] [Related]

  • 29. International Association for Law, Ethics and Science (the Milazzo group) convenes colloquium on "The law of 20 December 1988 on biomedical research: committees for the protection of persons or ethical committees?" (Paris, 21 Nov 1991).
    Byk C.
    Int Dig Health Legis; 1992 Mar; 43(2):393-7. PubMed ID: 11651638
    [No Abstract] [Full Text] [Related]

  • 30. New genetic medicine and public opinion.
    Howse JL.
    Forum Appl Res Public Policy; 1993 Mar; 8(3):29-33. PubMed ID: 11652663
    [No Abstract] [Full Text] [Related]

  • 31. US approves gene therapy on humans.
    Joyce C.
    New Sci; 1985 Oct 03; 108(1476):19. PubMed ID: 11655705
    [No Abstract] [Full Text] [Related]

  • 32. Safety boards must report their conclusions to IRBs.
    Maloney DM.
    Hum Res Rep; 1999 Oct 03; 14(10):3. PubMed ID: 11658061
    [No Abstract] [Full Text] [Related]

  • 33. Collaborative research involving human subjects: a survey of researchers using international single project assurances.
    Wichman A, Smith J, Mills D, Sandler AL.
    IRB; 1997 Oct 03; 19(1):1-6. PubMed ID: 11654738
    [No Abstract] [Full Text] [Related]

  • 34. Proposal for a good clinical practice directive.
    European Commission.
    Bull Med Ethics; 1998 Feb 03; No. 135():6-11. PubMed ID: 11657249
    [No Abstract] [Full Text] [Related]

  • 35. RU 486 and the politics of drug regulation in the United States and France.
    Kramnick RK.
    Cornell Int Law J; 1992 Feb 03; 25():667-718. PubMed ID: 11656340
    [No Abstract] [Full Text] [Related]

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