St. Lawrence University Institutional Review Board
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CITI Training for AY 2024-25:
Please be sure that you and your collaborators (including student researchers) have completed the CITI training. If you have completed the CITI training previously, please be sure that your certification is up to date by logging into your CITI account. No proposals or requests for continuation will be accepted for review without the appropriate CITI training.
If your participants are through the internet (e.g., MTurk), children, international, or in some other way pose special concerns, you will need to complete one or more additional modules in the CITI training. Please click on the link to CITI Program Training Information below for more information.
Meeting Dates and Deadlines
Below is the Spring 2025 IRB Meeting Schedule and Proposal Deadlines.
| Meeting Dates | Proposal Deadlines |
|---|---|
| January 28, 2025 | January 21, 2025 |
| February 4, 2025 | January 28, 2025 |
| February 18, 2025 | February 11, 2025 |
| March 4, 2025 | February 25, 2025 |
| March 25, 2025 | March 18, 2025 |
| April 8, 2025 | April 1, 2025 |
| April 22, 2025 | April 15, 2025 |
If you have any questions or concerns, please contact the IRB chair, Cathy Crosby at ccrosby@stlawu.edu or (315) 229-5167.
If you would like to attend the IRB meeting at which your proposal will be considered, please contact the IRB chair, Cathy Crosby.
Information about the IRB:
The role of the IRB is to insure that the autonomy and privacy of participants in research conducted by members of the St. Lawrence community are protected. Both the Code of Federal Regulations (Title 45, Part 46) and New York State Public Health Law (Article 24-A) require all proposed research involving human participants be approved by the institution’s IRB before it can proceed.
The principles which guide the IRB in its review and decision process are taken from the Policy Statement of the St. Lawrence University Institutional Review Board:
The IRB shall determine whether:
1) the risks to the participant are so outweighed by the sum of the benefit to the participant or the importance of the knowledge to be gained as to warrant a decision to allow the participant to accept these risks;
2) the rights and welfare of any such participants are adequately protected; and
3) legally effective informed consent is obtained from the participants by adequate and appropriate means.
To determine whether your project requires IRB approval: click here
Submitting an IRB Proposal:
Post-Approval Forms:
CITI Program Training:
Information for External Researchers