BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

293 related articles for article (PubMed ID: 11654437)

  • 1. Despite "clinical hold," subjects have right to keep getting experimental drug: Dahl v. HEM Pharmaceuticals Corporation (Part III).
    Maloney DM
    Hum Res Rep; 1996 Feb; 11(2):4-5. PubMed ID: 11654437
    [No Abstract]   [Full Text] [Related]  

  • 2. If a subject incurs obligations and carries them out, then consent is a contract: Dahl v. HEM Pharmaceuticals (Part II).
    Maloney DM
    Hum Res Rep; 1996 Jan; 11(1):4-5. PubMed ID: 11653221
    [No Abstract]   [Full Text] [Related]  

  • 3. Informed consent is binding contract: Dahl v. HEM Pharmaceuticals.
    Maloney DM
    Hum Res Rep; 1995 Dec; 10(12):4-5. PubMed ID: 11653220
    [No Abstract]   [Full Text] [Related]  

  • 4. Walking a thin line: distinguishing between research and medical practice during Operation Desert Storm.
    Schuchardt EJ
    Columbia J Law Soc Probl; 1992; 26(1):77-115. PubMed ID: 11651647
    [No Abstract]   [Full Text] [Related]  

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

  • 6. FDA's new rule on treatment use and sale of investigational new drugs.
    Levine RJ
    IRB; 1987; 9(4):1-4. PubMed ID: 11649946
    [No Abstract]   [Full Text] [Related]  

  • 7. Shaking up the status quo: how AIDS activists have challenged drug development and approval procedures.
    Dunbar MM
    Food Drug Cosmet Law J; 1991 Sep; 46(5):673-706. PubMed ID: 11651380
    [No Abstract]   [Full Text] [Related]  

  • 8. Considering experimentation and elusive truth: informed consent made difficult.
    Brodeur D
    Issues (St Louis Mo); 1992; 7(2):1-8. PubMed ID: 11659444
    [No Abstract]   [Full Text] [Related]  

  • 9. Can a court order participation in research?
    Holder AR
    IRB; 1987; 9(4):8-9. PubMed ID: 11649949
    [No Abstract]   [Full Text] [Related]  

  • 10. Emergency trials 'by popular consent.
    Kiernan V
    New Sci; 1995 Nov; 148(2002):6. PubMed ID: 11656475
    [No Abstract]   [Full Text] [Related]  

  • 11. Institutional review boards in the university setting: review of pharmaceutical testing protocols, informed consent and ethical concerns.
    Kobasic DM
    J Coll Univ Law; 1988; 15(2):185-216. PubMed ID: 11659168
    [No Abstract]   [Full Text] [Related]  

  • 12. Faith (healing), hope and charity at the FDA: the politics of AIDS drug trials.
    Annas GJ
    Villanova Law Rev; 1989 Sep; 34(5):771-97. PubMed ID: 11651162
    [No Abstract]   [Full Text] [Related]  

  • 13. Regulation of drug treatments for HIV and AIDS: a contractarian model of access.
    Salbu SR
    Yale J Regul; 1994; 11(2):401-53. PubMed ID: 11660141
    [No Abstract]   [Full Text] [Related]  

  • 14. A drug company report: what is the same and what is changing with respect to inclusion/exclusion of women in clinical trials.
    Goldmann BJ
    Food Drug Law J; 1993; 48(2):169-74. PubMed ID: 11653139
    [No Abstract]   [Full Text] [Related]  

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

  • 16. An update on the PEG-SOD study involving incompetent subjects: FDA permits an exception to informed consent requirements.
    Prentice ED; Antonson DL; Leibrock LG; Prabhu VC; Kelso TK; Sears TD
    IRB; 1994; 16(1-2):16-8. PubMed ID: 11652322
    [No Abstract]   [Full Text] [Related]  

  • 17. Getting new drugs to people with AIDS: a public policy response to Lansdale.
    Cohen MN
    Hastings Constit Law Q; 1991; 18(3):471-85. PubMed ID: 11651493
    [No Abstract]   [Full Text] [Related]  

  • 18. Experimental drugs: more of them, but they're no longer free.
    Caplan J
    Hastings Cent Rep; 1987 Jun; 17(3):3. PubMed ID: 11644019
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 15.