PIRB

                            Peoria Institutional Review Board

Research covers a wide variety of activities, it is highly recommended that you contact any member of our staff if you have questions regarding your project, what forms need to be submitted, and general requirements.  Otherwise, we have developed a guideline for new investigators: Guideline for new PI's

 

**Effective JULY 9th, 2007: New Reporting requirements for Unanticipated Events Involving Risks to Others. 

Word Format

Form Description

Submission Requirements: Detailed explanation on type of review, forms required, number of copies, deadlines and response time to investigative site.
Project/Protocol Review Form: Complete for initial submission of a research project, including requests for expedited review.
Responsibilities of Investigator Form: Complete for each new research project.
Continuing Review Form: Complete for continued review of approved research project.
Change in Research Form: Complete when submitting amendments, revised IBs, IC changes, advertising, etc.
Unanticipated Problems Involving Risks to Others: Please refer to worksheet above for reporting requirements/decisions.
UPIRSO Letter to Sponsor: This letter outlines OHRO's policies for reporting UPIRSOs.
Request for Exempt Review Form: Complete for request of exempt review.
Final Report Form: Complete to communicate closure of a study to PCIRB.
Sample Informed Consent Template (Updated 09/07/06)
Sample Tissue Banking Informed Consent Template (Updated 09/07/06)
Closed to Enrollment Form: Used to communicate to the IRB closure of enrollment for a particular study
Application for Waiver for Access to PHI for Retrospective Studies.

 

 

Application for Partial Waiver of Authorization for Screening/Recruitment Purposes and Preparatory to Research

 

 

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©1999 University of Illinois College of Medicine at Peoria - University of Illinois at Chicago

This page last updated on 07/25/07