These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

456 related items for PubMed ID: 11664810

  • 1. Informed consent to participate in research: Part II.
    Levine RJ.
    Bioethics Dig; 1977 Apr; 1(12):1-16. PubMed ID: 11664810
    [No Abstract] [Full Text] [Related]

  • 2. Protecting research subjects after consent: the case for the "research intermediary.
    Reiser SJ, Knudson P.
    IRB; 1993 Apr; 15(2):10-1. PubMed ID: 11651567
    [No Abstract] [Full Text] [Related]

  • 3. Informed consent process and document is criticized in court.
    Maloney DM.
    Hum Res Rep; 1994 Dec; 9(12):4-5. PubMed ID: 11654162
    [No Abstract] [Full Text] [Related]

  • 4. Research subject loses case against physician, IRB, and hospital.
    Maloney DM.
    Hum Res Rep; 1995 Feb; 10(2):4-5. PubMed ID: 11654160
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Ethics in neurobiological research with human subjects -- final reflections.
    Katz J.
    Account Res; 1996 Feb; 4(3-4):277-83. PubMed ID: 11654523
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Changing federal regulation of IRB's: the Commission's recommendations and the FDA's proposals.
    Levine RJ.
    IRB; 1979 Mar; 1(1):1-3+. PubMed ID: 11662736
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. IRBs and pharmaceutical company funding of research.
    Jellinek MS, Levine RJ.
    IRB; 1982 Oct; 4(8):9-10. PubMed ID: 11651693
    [No Abstract] [Full Text] [Related]

  • 11. Human experimentation: the review process in practice.
    Cowan DH.
    Case West Reserve Law Rev; 1975 Oct; 25(3):533-64. PubMed ID: 11661165
    [No Abstract] [Full Text] [Related]

  • 12. 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]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Informed consent in psychiatric research.
    Roth LH, Appelbaum PS, Lidz CW, Benson P, Winslade WJ.
    Rutgers Law Rev; 1987 Jul; 39(2-3):425-41. PubMed ID: 11659013
    [No Abstract] [Full Text] [Related]

  • 15. Federal agency's final rule says informed consent forms must be dated.
    Maloney DM.
    Hum Res Rep; 1996 Dec; 11(12):1-2. PubMed ID: 11655034
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. The FDA's enforcement of IRBs and patient informed consent.
    Kelsey FO.
    Food Drug Cosmet Law J; 1989 Jan; 44(1):13-20. PubMed ID: 11651627
    [No Abstract] [Full Text] [Related]

  • 18. Special informed consent requirements are included in protocol review procedures.
    Maloney DM.
    Hum Res Rep; 1995 Jul; 10(7):1-2. PubMed ID: 11654274
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Legal and financial encumbrances to clinical research.
    Sonnenreich MR.
    Perspect Biol Med; 1995 Jul; 23(2):. PubMed ID: 11663072
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 23.