St. Lawrence University Institutional Review Board

Welcome to the homepage for the Institutional Review Board (IRB) for St. Lawrence University!

You will find links to all of the information you need to submit a proposal or request continuation of an existing proposal. If you have questions or concerns, please contact the IRB chair, Dr. Cathy Crosby, at ccrosby@stlawu.edu or (315) 229-5167.

Please Note: As of the fall of 2016, all individuals submitting an IRB proposal or a request for continuation of prior approval are required to complete the CITI Program training. Please click on the links below for more information.

Spring Semester Meeting Dates and Deadlines:


February 1, 2018 (proposal deadline: January 25, 2018)
February 8, 2018 (proposal deadline: February 1, 2018)
February 22, 2018 (proposal deadline: February 15, 2018)
March 8, 2018 (proposal deadline: March 1, 2018)
March 29, 2018 (proposal deadline: March 22, 2018)
April 12, 2018 (proposal deadline: April 5, 2018)
April 26, 2018 (proposal deadline: April 19, 2018)

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.

Submitting an IRB Proposal:
Post-Approval Forms:
CITI Program Training:

Not sure whether your project requires IRB approval? Click here