| Human
Subjects Research: |
3
April 2013
Number of Applications Currently Under Review |
IRB
Review: 34 |
Exemption:
0 |
this can be used as an index to processing time |
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To comply with federal regulations and Miami policies, research
involving human subjects requires that researchers be familiar
with the ethical issues common to such work. In addition to
the required online training, all human subjects research must
be reviewed and the methods approved by an Institutional Review
Board (IRB).
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| Applications
for applying for IRB review of new planned research >
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| Applications
for modifying an approved protocol and annual continuing
research > |
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| Background
information and references> |
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When planning your submissions
to the IRB, please consider the annual chronology of IRB activity
shown to the left. Submissions in Feb-March and September-October
will be competing for board and compliance office time to a
greater extent than other months. |
IRB Co-Chairs
for academic year 2012-13:
Dr. Susan Cross Lipnickey and
Dr. Sarah Woodruff
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| To
report an adverse event involving research subjects: |
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Research Compliance Office (RCO):
Director: Dr. Neal Sullivan
(neal.sullivan@MiamiOH.edu)
Assistant Director: Ms. Jennifer Sutton (suttonja@MiamiOH.edu) |
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Multi-Agency
Federal Wide Assurance: |
- FWA 00000397 Expires
9 June 2014
- MU IORG ID: 0000563
Expires 9 Sep 2014
- MU IRB Registration ID: 00000895
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Institutional
Review Board for the Use of Human Subjects in Research (IRB):
In accordance with federal guidelines, the IRB
is charged with review of all research involving human subjects
at Miami. Each member of the Institutional Review Board is appointed
by the President of the University for a three year term. |
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