267 related articles for article (PubMed ID: 11655169)
1. FDA may "pull the plug" on consent waiver.
Ault A
Lancet; 1997 Oct; 350(9084):1084. PubMed ID: 11655169
[No Abstract] [Full Text] [Related]
2. Exception from informed consent for emergency research: drawing on existing skills and experience.
Davis AM
IRB; 1998; 20(5):1-8. PubMed ID: 11657584
[No Abstract] [Full Text] [Related]
3. Informed consent rule in USA will require more money.
Firshein J
Lancet; 1997 Jan; 349(9045):111. PubMed ID: 11654556
[No Abstract] [Full Text] [Related]
4. FDA revises informed consent regulations for emergency research.
Menasché A; Levine RJ
IRB; 1995; 17(5-6):19-22. PubMed ID: 11653359
[No Abstract] [Full Text] [Related]
5. Emergency trials 'by popular consent.
Kiernan V
New Sci; 1995 Nov; 148(2002):6. PubMed ID: 11656475
[No Abstract] [Full Text] [Related]
6. Proposal on waiver of informed consent poses major issues for research ethics.
Maloney DM
Hum Res Rep; 1997 Sep; 12(9):1-3. PubMed ID: 11660533
[No Abstract] [Full Text] [Related]
7. An even safer safety net.
Prentice E
Hastings Cent Rep; 1997; 27(3):46. PubMed ID: 11644996
[No Abstract] [Full Text] [Related]
8. FDA gets feedback on informed consent waiver.
Marwick C
JAMA; 1996 Feb; 275(5):347. PubMed ID: 8568998
[No Abstract] [Full Text] [Related]
9. Informed consent in the clinical research setting: experimentation on human subjects.
Owens JF
Med Trial Tech Q; 1987; 33(3):335-50. PubMed ID: 11653829
[No Abstract] [Full Text] [Related]
10. 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]
11. Protection of human subjects; new drugs for investigational use; conforming amendments; final rule.
U.S. Food and Drug Administration
Fed Regist; 1984 Oct; 49(212):43637-8. PubMed ID: 11645532
[No Abstract] [Full Text] [Related]
12. Protection of human subjects; informed consent; standards for institutional review boards for clinical investigations; and clinical investigations which may be reviewed through expedited review procedures.
U.S. Food and Drug Administration
Fed Regist; 1981 Jan; 46(17):8942-80. PubMed ID: 11658611
[No Abstract] [Full Text] [Related]
13. Ban on medical experiments without consent is relaxed.
Kolata G
N Y Times Web; 1996 Nov; ():A1, C6. PubMed ID: 11647142
[No Abstract] [Full Text] [Related]
14. OPRR and FDA propose revised expedited review categories.
McGough H
IRB; 1998; 20(1):9, 11. PubMed ID: 11655326
[No Abstract] [Full Text] [Related]
15. 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]
16. Protection of human subjects; informed consent; proposed rule.
U.S. Food and Drug Administration
Fed Regist; 1995 Sep; 60(183):49086-103. PubMed ID: 11656433
[No Abstract] [Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. Research in the emergency department.
Lears L
Health Care Ethics USA; 1997; 5(2):4-5. PubMed ID: 11657187
[No Abstract] [Full Text] [Related]
[Next] [New Search]
