Consent for continuing research participation: what is it and when should it be obtained?
IRB
.
2002 May-Jun;24(3):1-6.
Authors
Dave Wendler
1
,
Jonathan Rackoff
Affiliation
1
Department of Clinical Bioethics, National Institutes of Health, Bethesda, MD, USA.
PMID:
12848185
No abstract available
MeSH terms
Disclosure / standards
Dissent and Disputes
Ethics Committees, Research
Human Experimentation / standards*
Humans
Informed Consent / standards*
Research Subjects
Time Factors*