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Journal Abstract Search

394 related items for PubMed ID: 11655326

  • 1. OPRR and FDA propose revised expedited review categories.
    McGough H.
    IRB; 1998; 20(1):9, 11. PubMed ID: 11655326
    [No Abstract] [Full Text] [Related]

  • 2. Two rules on expedited IRB reviews are final.
    Maloney DM.
    Hum Res Rep; 1999 Jan; 14(1):3. PubMed ID: 11657557
    [No Abstract] [Full Text] [Related]

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

  • 4. Fears mount for gene scrutiny as watchdog faces axe.
    Kiernan V.
    New Sci; 1996 Jun 08; 150(2033):10. PubMed ID: 11656540
    [No Abstract] [Full Text] [Related]

  • 5. FDA revises informed consent regulations for emergency research.
    Menasché A, Levine RJ.
    IRB; 1995 Jun 08; 17(5-6):19-22. PubMed ID: 11653359
    [No Abstract] [Full Text] [Related]

  • 6. Institutional review board approval required by rule.
    Maloney DM.
    Hum Res Rep; 1996 Aug 08; 11(8):3. PubMed ID: 11654440
    [No Abstract] [Full Text] [Related]

  • 7. Commission says institutional review boards should change procedures now.
    Maloney DM.
    Hum Res Rep; 1999 Jan 08; 14(1):1-2. PubMed ID: 11657555
    [No Abstract] [Full Text] [Related]

  • 8. The history of institutional review boards.
    Sherman M, Van Vleet JD.
    Regul Aff J; 1991 Jan 08; 3():615-27. PubMed ID: 11651491
    [No Abstract] [Full Text] [Related]

  • 9. The concept of the IRB and bureaucratic reality: an exchange of letters.
    van Eys J, Levine RJ.
    IRB; 1984 Jan 08; 6(4):8-10. PubMed ID: 11649563
    [No Abstract] [Full Text] [Related]

  • 10. National commission proposes numerous new regulations of institutional review boards.
    Maloney DM.
    Hum Res Rep; 1998 Oct 08; 13(10):1-2. PubMed ID: 11657739
    [No Abstract] [Full Text] [Related]

  • 11. The changing clinical trials scene: the role of the IRB.
    Mitchell SC, Steingrub J.
    IRB; 1988 Oct 08; 10(4):1-5. PubMed ID: 11650078
    [No Abstract] [Full Text] [Related]

  • 12. Federal report says protection of human subjects is threatened by numerous factors.
    Maloney DM.
    Hum Res Rep; 1996 May 08; 11(5):1-3. PubMed ID: 11654438
    [No Abstract] [Full Text] [Related]

  • 13. Informed consent process is deemed "legally and ethically invalid" by witness.
    Maloney DM.
    Hum Res Rep; 1995 Jan 08; 10(1):4-5. PubMed ID: 11660008
    [No Abstract] [Full Text] [Related]

  • 14. Annual review: observed deficiencies and suggested corrections.
    Adams MS, Conrad DA.
    IRB; 1996 Jan 08; 18(6):1-4. PubMed ID: 11654743
    [No Abstract] [Full Text] [Related]

  • 15. Research compliance changes will affect rules on protection of human subjects.
    Maloney DM.
    Hum Res Rep; 1999 May 08; 14(5):1-2. PubMed ID: 11657776
    [No Abstract] [Full Text] [Related]

  • 16. The impact of institutional review boards on clinical research.
    Levine RJ.
    Perspect Biol Med; 1999 May 08; 23(2):. PubMed ID: 11663073
    [No Abstract] [Full Text] [Related]

  • 17. Special informed consent requirements are included in protocol review procedures.
    Maloney DM.
    Hum Res Rep; 1995 Jul 08; 10(7):1-2. PubMed ID: 11654274
    [No Abstract] [Full Text] [Related]

  • 18. An overview of FDA, IRBs and regulations.
    Petricciani JC.
    IRB; 1981 Dec 08; 3(10):1-3, 11. PubMed ID: 11649413
    [No Abstract] [Full Text] [Related]

  • 19. Proposal on waiver of informed consent poses major issues for research ethics.
    Maloney DM.
    Hum Res Rep; 1997 Sep 08; 12(9):1-3. PubMed ID: 11660533
    [No Abstract] [Full Text] [Related]

  • 20. Human experimentation: the review process in practice.
    Cowan DH.
    Case West Reserve Law Rev; 1975 Sep 08; 25(3):533-64. PubMed ID: 11661165
    [No Abstract] [Full Text] [Related]

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