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IRB Frequently Asked Questions – FAQ

• Where do I submit my IRB application?

  Applications are submitted through the web-based research administration system, Streamlyne.  Streamlyne can be accessed at:

• Who is responsible for ethical conduct in research with human subjects?

  The primary responsibility for maintaining ethical standards and protecting human rights rests with individual researchers and research advisors. The Institutional Review Board (IRB) offers an added measure of assurance and serves as a local resource for the interpretation of ethical guidelines.

• What is the responsibility of the Institutional Review Board?

  The IRB is a committee, charged by Â鶹´«Ã½'s Institutional Official (IO) for the Protection of Human Research Subjects, with the responsibility for reviewing all proposed research involving human subjects for adherence to ethical standards. IRB members work with individual researchers to ensure that federal and university policies are followed and that human rights are safeguarded.

• What kinds of research are subject to review by the IRB?

  The federal regulations governing research using human subjects define research as "a systematic investigation, including research development, testing, and evaluation, designed to develop or contribute to generalizable knowledge." Research is subject to IRB review when an investigator, in the course of conducting research, obtains:
  • Data through intervention or interaction with a living individual or

  • Identifiable private information about a living individual Examples of generalized knowledge include, but are not limited to (1) studies being conducted with the intent of publishing journal articles; (2) theses, dissertations, or other investigations that will be biographically available (3) research that is presented at conferences or other professional venues; and (4) pilot studies that form the bases of subsequent research or are conducted in collaboration with investigators from other institutions.

  Students who present research data as part of in-class presentations may need to obtain IRB approval if they are also intending to present their results at conferences or submit their papers for publication.

  Research that analyzes archival records from individuals may also be subject to review by the IRB. Evaluations of workshops and programs are not considered "research" if results are not to be distributed outside the institutional setting.

• Who is obligated to follow IRB procedures?

   All Â鶹´«Ã½ faculty, staff, and students who conduct research with human subjects are obligated to follow Â鶹´«Ã½ policies and procedures.

• What kinds of reviews are conducted?

  Protocol applications for IRB review fall into three categories. Before completing an IRB protocol, investigators are advised to thoroughly study the IRB guidelines to determine the type of review their research will require - exempt, expedited, or full-board review.

  Each of these three categories of review has specific guidelines for submission, and receives different levels of scrutiny during review.

  Please refer to the Procedures for Research Involving Human Participants for more information.

• How do IRB members review proposed research?

  IRB members have been trained in ethical principles and in Â鶹´«Ã½ procedures governing humans subjects in research. They review applications to ensure that all information specified in the guidelines is included. Paying close attention to principles of ethical conduct, IRB members examine applications to ensure that risk and harm are minimized; benefits to science, humanity, and research subjects are maximized; the autonomy and privacy rights of subjects are protected; and the cost and benefits of research are fairly distributed among persons and groups. IRB members examine consent forms particularly closely to ensure that the necessary language and instructions are included and that subjects are fully informed of the risks as well as their rights.

•  Who is on the IRB?

  The IRB is comprised of Â鶹´«Ã½ faculty members with diverse disciplinary and methodological expertise. In addition, the board includes a community member and a non-scientific member in accordance with federal regulation. The Office of Research & Sponsored Programs provides administrative supports. Current IRB membership.

• What if my research involves collaborators at other institutions who have received IRB approval from their institutions?

  Â鶹´«Ã½ faculty members and students who are collaborating with individuals at another institution must attach a copy of the other institution's approved IRB protocol with their Â鶹´«Ã½ protocol applications. The Â鶹´«Ã½ IRB will usually confirm that adequate provisions have been taken to protect the rights of human participants through a review of the other institution's approved protocol, although occasionally the Â鶹´«Ã½ IRB may find it necessary to ask for clarification. In some cases, Â鶹´«Ã½ or the other collaboration institution may function as the authorized agent for IRB review for both institution. Â鶹´«Ã½ IRB Chair and the IRB administrator at ORSP can provide additional information.

• What other kinds of permission are needed?

  Written permission from appropriate authorities (individuals who are authorized to make commitments on behalf of another organization or institution) is required when researchers collect data in other institutions. Examples include schools, child care centers, hospitals, sports arenas, shopping malls, and other universities. This signed letter of permission must be submitted as part of the IRB protocol applications.

• What if my students need to conduct research as a class assignment?

  IRB procedures include provisions for instructors who require student to conduct research in class as part of an omnibus arrangement. Please refer to the description of Classroom Research and the Procedures of Research Involving Human Participants for detailed information.