The University of Rhode Island Institutional Review Board (IRB) reviews research projects which involve human subjects to ensure that two broad standards are upheld: first, that subjects are not placed at undue risk; second, that they give uncoerced, informed consent to their participation.
With representation from a wide range of scientific disciplines and from outside the academic community, the IRB gives individualized attention to the numerous research projects at the University.
Protocol Review Process
The length of the approval process is influenced by several varying factors, such as the complexity of a protocol, the risk of the project to the research subjects, and the completeness of documentation. In all circumstances, early submission combined with accurate documentation will result in an expedited approval.
The IRB application process starts with your submission of the application form, consent forms and other required appendices/materials. The ORI staff pre-reviews your application to make sure all of the necessary materials are there for IRB review. The ORI staff will contact you by email if your application or forms are not sufficient and will let you know what needs to be done to get your application ready for review by the IRB.
Applicants must submit application materials to the IRB at least three weeks prior to the date of the scheduled IRB meeting for all protocols that must be reviewed by the fully convened IRB. Please allow at least 6-8 weeks for protocol review, depending on the complexity of the project, the risk of the project to the research subjects, and the extent of revisions required.
Submission Process and Forms
New IRB Forms effective July 3, 2014
Effective July 3, 2014, URI's Institutional Review Board (IRB) for human subject research protection will begin using a new set of IRB forms for submission. Currently, both the old set of IRB forms, and new set of forms are available. The old IRB forms are available on the URI research website: http://www.uri.edu/research/tro/about/IRB/forms.html
The new forms may be used now, prior to the July 3, 2014 implementation date at the PI discretion. The new forms are available within the online portal URI uses for all IRB submissions, IRBNet.org under Forms and Templates.
After July 3, 2014, old versions of the IRB forms will be removed from the web and will no longer be accepted. The new IRB forms are created on Adobe Acrobat. Macintosh users MUST use Adobe Reader (as opposed to Adobe Professional) for form completion.
The Initial Review of Human Subject Research (Initial IRB Application) is required for all research that requires a human subject component (exempt, expedited, and full convened IRB review). What you will notice immediately is the there are many appendices to the Initial IRB Application. Most Principal Investigators (PIs), will seldom use beyond a handful of these. These forms have designed to streamline the review process so all information required for review is submitted at time of application. Our hope is to decrease the review time for researchers
The Office of Research Integrity will be offering a workshop to introduce, explain, and answer questions of researchers and students regarding the new IRB forms. See the IRB Workshops flyer for more details regarding this event and other IRB workshops hosted by ORI.
All information must be submitted through IRBNet. Refer to the link below for required forms and sample documents.
Human Subjects Research Training