Institutional Review Board
PLEASE NOTE: all materials must be submitted in full and in the appropriate format by the corresponding submission deadline in order to be included at the full board meeting date posted. All documents should be submitted as a single pdf attachment to firstname.lastname@example.org.
FULL BOARD MEETING DATES ARE AS FOLLOWS:
Submission Deadline: 2/11 (M) --protocols received by this date will be reviewed by 2/20
Submission Deadline: 2/18 (M) --protocols received by this date will be reviewed by 3/6 or 3/13
Submission Deadline: 3/11 (M) --protocols received by this date will be reviewed by 3/20 or 3/27
Submission Deadline: 4/15 (M) --protocols received by this date will be reviewed by 4/24
-All exempt and expedited summer submissions will be reviewed; however, the timeline for review will be longer than usual. If you have a sensitive timeline, please contact the IRB to determine whether we will be able to accommodate that timeline.
-ALL submissions after September 1, 2017 must include a copy a Training Certificates for all PIs, Co-PIs and other individuals involved in human subjects research. The NIH Training used in the past is no longer available. While we find a permanent replacement, all PIs, Co-PIs and other individuals involved in the research project should complete the TCPS2 CORE training available here: http://tcps2core.ca/welcome
NOTE: A training certificate will be provided a the end and should be submitted with the IRB protocol.
-A student handbook is available below. This handbook provides important details on putting your IRB protocol together, how to submit the protocol, and the review process.
Research that involves active, human participants might be required to be submitted to a review process that ensures the best data, safety for participating subjects, and best research practices.
Institutional Review Board (IRB) review is required when:
- research involves exposing active human participants to psychological, physical, or any other kind of harm
- research is a systematic investigation—including research development, testing, and evaluation,—designed to develop or contribute to generalizable knowledge
IRB approval is not required when data collection is part of:
- normal educational practices
- journalistic surveys or interviews
- oral histories, biographies, or case studies not meant for generalizeable purposes
- institutional or quality assessment
Projects that do not require IRB review might still present risks to human participants and thus call for the assurance of ethical principles and protocol.
Researchers and faculty advisors have primary responsibility for ensuring that any activities involving human participants are handled ethically.
If unsure about IRB review, please contact the IRB Chair to assist in deciding how to proceed.
- IRB Review Timeline, Request, and Paperwork
- Submit the completed Protocol Request Form to IRB@cabrini.edu.
- All materials must be submitted electronically in one PDF.