The Institutional Review Board provides oversight to research involving human participants and ensures that guidelines are followed that protect the rights and safety of these participants.
The Alma College Institutional Review Board (IRB) must review and approve any formal research study involving human subjects before the study begins. It is the responsibility of the IRB to protect the rights and safety of research subjects. The board reviews all proposed studies in order to ensure that research is conducted at Alma College, or by College personnel, in a manner consistent with the principles of the Belmont Report and all applicable laws.
If you have questions regarding the IRB, please contact Dr. Alex Montoye at email@example.com or (989) 463-7923.
Policies and Procedures and IRB Application
- Human Subjects Research Restrictions Related to COVID-19
- IRB Policies and Procedures
- We recommend that you complete your IRB application in this template, and then copy and paste your responses into Qualtrics when ready to submit. If you start an application in Qualtrics but do not submit it, it may not save, so completing in the Word document will ensure that you do not lose your work.
- Qualtrics Policies
2020-2021 IRB Meeting Dates and Application Submission Deadlines
|Meeting Date||Application Submission Date|
|January 15, 2021||January 1, 2021|
|February 12, 2021||January 29, 2021|
|March 12, 2021||February 26, 2021|
|April 9, 2021||March 26, 2021|
2020-2021 IRB Membership Roster
|Dr. Alex Montoye||Chair||Faculty, IPHS|
|Dr. Phil Andre||Assistant to the Chair||Faculty IPHS|
|Dr. Mark Mills||Secretary||Faculty, Psychology|
|Dr. Kate Blanchard||Member||Faculty, Philosophy and Religious Studies (non-scientist)|
|Laura Jean Francois||Member||Faculty, Nursing|
|Dr. Hyun Kim||Member||Faculty, IPHS|
|John MacArthur||Member||Director of Institutional Research (non-scientist)|
|Sue Malone||Member||Community member (unaffiliated with Alma College; non-scientist)|
|Dr. Jessie Store||Member||Faculty, Education|
Examples of Informed Consent Documents
Federal Protection of Human Subjects
United States federal law CFR Title 45: Public Welfare, Part 46: Protection of Human Subjects, or the “Common Rule,” was originally passed by congress in 1974. This law sets forth the basic ethical principles that should underlie the conduct of biomedical and behavioral research involving human subjects and provides guidelines which should be followed to assure that such research is conducted in accordance with those principles.
The Belmont Report
The Belmont Report is a condensed summary of the basic ethical principles identified by the Commission in the course of its deliberations. It is the product of lengthy discussions held in February 1976 at the Smithsonian Institution’s Belmont Conference Center. The findings are supplemented by subsequent discussions within the Commission over a period of nearly four years. It is a statement of basic ethical principles and guidelines that should guide resolution of ethical problems that surround the conduct of research with human subjects. The report was published in 1979.