Whitworth Home Page > Sponsored Programs >
Institutional Review Board Form Instructions,
Institutional Review Board Proposal
Prior to undertaking your research project, you must have your project proposal reviewed and approved by Whitworth’s Institutional Review Board (IRB). This is in everybody’s best interests – it helps ensure that you, your participants, and the university are conducting safe, worthwhile research.
You or your research group should prepare a draft of the proposal to submit to the IRB committee. The committee encourages you to have your proposal draft reviewed in advance by your supervising faculty member; this will facilitate preparation of an accurate, appropriate, and sufficiently detailed application. In light of this, the IRB application form found online has been recreated in this document specifically to help you prepare your application.
The information at the link will provide instructions that make the submission process understandable and will mitigate technical difficulties. Please read through all of these instructions. Once you have finished reading the instructions, click on “IRB Application” at the bottom of the page.
SharePoint Log-In Instructions (required to open a new IRB form):
Flowchart for an IRB Form:
1) Investigator submits and signs form; > 2) ALL submitters sign; > 3) faculty assurance reviews and signs; > 4) form review; > 5) protocol-change request may be made; > 5) protocol changes are made, and ALL investigators sign again; > 6) FINAL review by board.
IRB form or process questions go to Lynn Noland. Technical questions re: SharePoint access should be sent to email@example.com.
The Institutional Review Board meets weekly, on Fridays at 3:30. If your form requires a full board review, your application MUST be submitted by the Monday prior to the Friday meeting. See the Sponsored Programs page for a schedule of the Friday meetings.
Policy on the Use of Alcohol/Controlled Substances/OTC Drugs in Student Research (Approved 11/16/12)
The IRB will not approve student research projects using any controlled substance including alcohol and prescription drugs. Projects using over-the-counter (OTC) drugs and supplements must include a complete, literature-based risk-assessment plan that details all potential side effects and health risks of the drug, and includes a protocol for minimizing and mitigating said risks should they occur in a study participant. The risk-assessment plan must be a minimum of one single-spaced page based on at least five references from the primary scientific literature. The IRB reserves the right to reject any proposal using OTC drugs that does not have a sufficient risk-assessment plan.
Recruiting Subjects at Other Institutions
If you would like to use subjects from Eastern Washington University or Gonzaga University, please contact one of the following department chairs to determine the process needed:
EWU: Sarah Keller, Ph.D., IRB Chair and Professor of Anthropology
Gonzaga: Deborah Booth, Ph.D., Chair and Associate Professor of Teacher Education