Campus

GENERAL INFORMATION

FOR RESEARCHERS

FOR IRB MEMBERS

Welcome to Marquette University's Institutional Review Board (IRB) for the protection of human subjects. The MU IRB reviews and approves research involving the use of human subjects under the jurisdiction of Marquette University. The IRB is charged with the responsibility of ensuring the adequacy of the research plan, to minimize risks and to maximize the potential for benefit from human subjects’ who participate in research based on federal and state regulations, in addition to institutional policies.

ANNOUNCEMENTS

07/13/2018- The Office of Human Research Protections has made several revisions to the regulations governing human research protections. A few minor changes will be implemented as of 07/19/2018 and the remaining changes will be implemented on 1/20/2019. For more information, please see the FAQ document the IRB office has created. Any questions can be addressed to Jessica Rice, the IRB Manager.

**The continuing review submission form has been updated to reflect the new regulations and is required for all continuing review submissions submitted after 07/19/2018. Please see our forms and templates page for the new form***

03/15/2018 - A revised protocol form has been created. This form should be used with any study type (exempt, expedited or full board). A new amendment form has also been developed. Both of these revised forms are available on our forms and templates page.

08/28/2017 - Beginning August 2017, the IRB will be using the KUALI research software for IRB office record management. If the PI is an undergraduate student, the student must complete the Update KUALI Research Student Group: Undergraduate form and submit it to the Office of the Registrar in order to grant permission to allow undergraduate student information to be stored in the research software.

04/27/2017 - New guidance documents are available to provide helpful information to researchers. Visit the Useful Links page for guidance documents on the use of online surveys in research, issues surrounding genetic testing and helpful hints on how to deidentify your dataset.

09/08/2016 - New human subjects training available. The IRB has switched from the NIH online training modules to CITI. Visit the Training & Education page for more information.

06/14/2016 - MU School of Dentistry (MUSoD) approval required for all new IRB submissions where MUSoD students and patients will be research subjects. Complete the MUSoD IRB Approval Form and obtain MUSoD approval prior to IRB submission. A copy of the approval must be included with the IRB submission. Contact Dr. Andrew Dentino for more information.

08/28/2014 - Need to add research assistants or other personnel to your protocol? Check out the Personnel Amendment Form. Changes to personnel are normally approved in a few business days. Don't forget to check the Training & Education page for training requirements and instructions for formatting certificates.


SITE MENU

Schroeder Complex

Mission Statement

The mission of the Office of Research Compliance, in cooperation with and in support of the Institutional Review Board, Institutional Animal Care and Use Committee, Radiation Safety Committee, and Institutional Biosafety Committee, is to facilitate safe and ethical research conducted by Marquette faculty, staff and students in the areas of human subjects, animal subjects, radiation safety and biosafety.