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 *

483 related articles for article (PubMed ID: 11878337)

  • 1. European Union clinical trials directive.
    Bull Med Ethics; 2001 Jul; (169):13-24. PubMed ID: 11878337
    [No Abstract]   [Full Text] [Related]  

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

  • 3. European directive on clinical trials.
    Bull Med Ethics; 1999 May; No. 148():3-4. PubMed ID: 11657983
    [No Abstract]   [Full Text] [Related]  

  • 4. Informed consent in clinical research: policies and practices in Singapore.
    Ramachandran AJ
    J Biolaw Bus; 2003; 6(1):65-75. PubMed ID: 15239181
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Medical Research Involving Human Subjects Act.
    Netherlands
    Bull Med Ethics; 1999 Nov; No. 152():13-8. PubMed ID: 11658081
    [No Abstract]   [Full Text] [Related]  

  • 6. European Commission considers revisions to clinical trials directive.
    Mason E
    J Natl Cancer Inst; 2010 Mar; 102(5):292-4, 297. PubMed ID: 20173121
    [No Abstract]   [Full Text] [Related]  

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

  • 8. Establishing pan-European clinical trials: regulatory compliance and other practical considerations.
    Grienenberger A
    J Biolaw Bus; 2004; 7(4):58-63. PubMed ID: 15675097
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Children as research subjects: a proposal to revise the current federal regulations using a moral framework.
    Ross LF
    Stanford Law Pol Rev; 1997; 8(1):159-76. PubMed ID: 16528858
    [No Abstract]   [Full Text] [Related]  

  • 10. Guidelines Relevant to the Procedure for Conduct of Clinical Trials.
    Ireland. National Drugs Advisory Board
    Int Dig Health Legis; 1987; 38(2):376-83. PubMed ID: 11649270
    [No Abstract]   [Full Text] [Related]  

  • 11. Clinical trials face heightened scrutiny as science and commerce appear to merge.
    Lorman AJ
    J Biolaw Bus; 2001; 4(4):23-32. PubMed ID: 12751494
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Research column: protection of children as subjects in research.
    Nelson AE
    J Pediatr Oncol Nurs; 2003; 20(3):141-3. PubMed ID: 12776262
    [No Abstract]   [Full Text] [Related]  

  • 13. New federal rule on protecting children as research subjects.
    Maloney DM
    Hum Res Rep; 2001 Jun; 16(6):3. PubMed ID: 11785526
    [No Abstract]   [Full Text] [Related]  

  • 14. [Opinion of the French National Academy of Medicine on the legislative framework for the application of the European Directive on biomedical research in humans].
    Rouëssé J
    Bull Acad Natl Med; 2003; 187(5):1001-15. PubMed ID: 14979061
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Regulations of the ethical evaluation system of scientific and clinical research in connection with Poland joining the European Union].
    Raszeja S
    Arch Med Sadowej Kryminol; 2004; 54(2-3):151-4. PubMed ID: 15495560
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Achieving proper balance in research with decisionally-incapacitated subjects: NAMI's perspectives on the working group's proposal.
    Flynn LM; Honberg RS
    J Health Care Law Policy; 1998; 1(1):174-92. PubMed ID: 15573436
    [No Abstract]   [Full Text] [Related]  

  • 17. Regulation of research on the decisionally impaired: history and gaps in the current regulatory system.
    Moreno JD
    J Health Care Law Policy; 1998; 1(1):1-21. PubMed ID: 15573427
    [No Abstract]   [Full Text] [Related]  

  • 18. Informed consent for Alzheimer's disease clinical trials: a survey of clinical investigators.
    Karlawish JH; Knopman D; Clark CM; Morris JC; Marson D; Whitehouse PJ; Kawas CH
    IRB; 2002; 24(5):1-5. PubMed ID: 12737167
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. European move affects academic trials research.
    Sinha G
    J Natl Cancer Inst; 2006 Aug; 98(16):1100-1. PubMed ID: 16912258
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 25.