This panel will consider how to think about risk to bystanders in research. Among the questions that will be discussed are: Should IRBs take bystander risk into account when approving studies? If so, to what sorts of protections are bystanders entitled? Are there upper limits of risk that we can impose on non-participants in research? What are the potential kinds of harm to non-participants in research?
PANELISTS:
Daniel Wikler, PhD
Mary B. Saltonstall Professor of Population Ethics and Professor of Ethics and Population Health, Harvard T.H. Chan School of Public Health
Alayna Tackett, PhD
Pediatric Psychologist and Assistant Professor in the Division of Medical Oncology, OSU
Katherine Walton, PhD
Associate Professor of Psychology and Psychiatry, OSU
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