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Research@UIC > Protocol
Review >
IRB > Getting Started
Getting Started
A
Guide for Investigators and Research Staff
Who is required to submit
an IRB application?
The UIC IRBs have jurisdiction over the following categories of research
when that research involves the use of human subjects, or identifiable
private data or tissues derived from human subjects, and the institution
is “engaged”in
the research by the nature of the research activities:
- Research conducted by UIC faculty and staff.
- Research conducted by adjunct faculty, such as non-salaried faculty, in their role as an adjunct faculty member.
- Research conducted by students, including research to satisfy a requirement
imposed by UIC for the award of a degree or the completion of a course
of study.
- Research performed on the premises of UIC, or using equipment belonging
to UIC.
- Research involving the use or disclosure of UIC protected health information
or other identifiable private information.
- Research funded by or supported through UIC.
- The UIC IRBs do not exercise
authority or responsibility for research when UIC is not engaged in the
research or research not involving human subjects. The IRB’s
jurisdiction extends to research in the social/behavioral sciences (i.e.
survey, education, public health), as well as to research in the health/biological
sciences (i.e. clinical trials, tissue collection, medical chart review).
The IRB’s authority extends
to all human subject research, regardless of the funding source, including
unfunded and departmentally funded research.
Engagement in the
research is determined using the OHRP guidance document, “Engagement
of Institutions in Research,” located at www.hhs.gov/ohrp/humansubjects/guidance/engage08.html.
Masters
of Public Health (MPH) Capstone projects that are only submitted in writing
to faculty reviewers and/or presented at a forum open only to the School
of Public Health (SPH) community do not require IRB review and approval.
However, if MPH students plan to submit their capstone paper for publication
or for presentation at meetings open to the public (e.g., a regional
conference), they must seek the appropriate level of review through
OPRS and the IRB, as they may be conducting human subjects research.
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