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References
1.Department of Clinical Bioethics at the National Institutes of Health. Guidelines for Writing Informed Consent Documents. Ethical and Regulatory Aspects of Human Subjects Research. Washington, DC : Department of Clinical Bioethics at the National Institutes of Health ; 1999 .
2.
Sharp
R
. Obtaining informed consent . NIEHS IRB Bulletin 3 , 2000 ; 1 –4 . Available at: http://dir.niehs.nih.gov/direb/irb/irb_bulletin3.htm. Accessed November 2001.
3.
Powers
M
. Publication-related risks to privacy: Ethical implications . Hastings Cent Rep. 1993 ;15 (4 ):7 –11 .
4.
Warnock
M
. Informed consent: A publisher's duty . BMJ. 1998 ;316 :1002 –1003 .
5.ICMJE. Uniform requirements for manuscripts submitted to biomedical journals. Available at: http://www.icmje.org. Accessed July 21, 2002.
6.
Yank
V
Rennie
D
. Reporting of informed consent and ethics committee approval in clinical trials . JAMA. 2002 ;287 :2835 –2838 .
7.
Amdur
RJ
Biddle
C
. Institutional Review Board approval and publication of human research results . JAMA. 1997 ; 277 :909 –914 .
