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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

108 related articles for article (PubMed ID: 20445198)

  • 1. Institutional review boards, professionalism, and the internet.
    Martensen R
    Sci Transl Med; 2010 May; 2(30):30cm15. PubMed ID: 20445198
    [TBL] [Abstract][Full Text] [Related]  

  • 2. New federal guidance adds duties for institutional review boards (IRBs).
    Maloney DM
    Hum Res Rep; 2005 Nov; 20(11):1-2. PubMed ID: 16358479
    [No Abstract]   [Full Text] [Related]  

  • 3. Informed consent and approval by institutional review boards in published reports on clinical trials.
    Ruiz-Canela M; Martínez-González MA; Gómez-Gracia E; Fernández-Crehuet J
    N Engl J Med; 1999 Apr; 340(14):1114-5. PubMed ID: 10206829
    [No Abstract]   [Full Text] [Related]  

  • 4. Preventive ethics for including women of childbearing potential in clinical trials.
    McCullough LB; Coverdale JH; Chervenak FA
    Am J Obstet Gynecol; 2006 May; 194(5):1221-7. PubMed ID: 16647904
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Randomized, controlled trials as minimal risk: an ethical analysis.
    Morris MC; Nelson RM
    Crit Care Med; 2007 Mar; 35(3):940-4. PubMed ID: 17255879
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ten questions institutional review boards should ask when reviewing international clinical research protocols.
    Fitzgerald DW; Wasunna A; Pape JW
    IRB; 2003; 25(2):14-8. PubMed ID: 12833903
    [No Abstract]   [Full Text] [Related]  

  • 7. [Responsibilities of ethics committees].
    von Bergmann K
    Med Klin (Munich); 2000 May; 95(1 Spec No):15-7. PubMed ID: 10851843
    [TBL] [Abstract][Full Text] [Related]  

  • 8. E-recruitment based clinical research: notes for Research Ethics Committees/Institutional Review Boards.
    Refolo P; Sacchini D; Minacori R; Daloiso V; Spagnolo AG
    Eur Rev Med Pharmacol Sci; 2015; 19(5):800-4. PubMed ID: 25807433
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Institutional review boards not sufficiently monitoring recruitment of human subjects.
    Maloney DM
    Hum Res Rep; 2000 Aug; 15(8):1-3. PubMed ID: 12199290
    [No Abstract]   [Full Text] [Related]  

  • 10. Ethics of clinical trials for research ethics boards: proceedings of a national workshop.
    National Council on Bioethics in Human Research (Canada)
    NCBHR Commun; 1991; 2(2):4-23. PubMed ID: 11659919
    [No Abstract]   [Full Text] [Related]  

  • 11. Variation in standards of research compensation and child assent practices: a comparison of 69 institutional review board-approved informed permission and assent forms for 3 multicenter pediatric clinical trials.
    Kimberly MB; Hoehn KS; Feudtner C; Nelson RM; Schreiner M
    Pediatrics; 2006 May; 117(5):1706-11. PubMed ID: 16651328
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Barriers to conducting clinical research in reproductive medicine: India.
    Pai H
    Fertil Steril; 2011 Oct; 96(4):809-10. PubMed ID: 21961915
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Institutional review boards should require clinical trial registration.
    Levin LA; Palmer JG
    Arch Intern Med; 2007 Aug 13-27; 167(15):1576-80. PubMed ID: 17698679
    [No Abstract]   [Full Text] [Related]  

  • 14. The process of clinical trials: a model for successful clinical trial participation.
    Lengacher CA; Gonzalez LL; Giuliano R; Bennett MP; Cox CE; Reintgen DS
    Oncol Nurs Forum; 2001 Aug; 28(7):1115-20. PubMed ID: 11517845
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Current status of research on the federal guidelines for performing research using an exception from informed consent.
    Schmidt TA; Lewis RJ; Richardson LD
    Acad Emerg Med; 2005 Nov; 12(11):1022-6. PubMed ID: 16264068
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Informed consent: process and clinical issues.
    Berry DL; Dodd MJ; Hinds PS; Ferrell BR
    Oncol Nurs Forum; 1996 Apr; 23(3):507-12. PubMed ID: 8801511
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Ethics committees bear a responsibility for patient information. Informed consent implies that the patient understands what he has consented to].
    Werkö L
    Lakartidningen; 2002 Mar; 99(14):1552-5. PubMed ID: 12025208
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ethical issues in administrative continuous improvement. Applying the concept of prior notification to the conduct of firm trials.
    Goldberg HI
    Med Care; 1990 Sep; 28(9):822-33. PubMed ID: 2205768
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 26(1):1-47. PubMed ID: 16514756
    [No Abstract]   [Full Text] [Related]  

  • 20. Comparison of German and American law concerning clinical trials.
    Deutsch E
    Pediatr Pharmacol (New York); 1983; 3(3-4):353-9. PubMed ID: 6677881
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.