Peoria Institutional Review Board
EFFECTIVE APRIL 1ST, 2007:

Requirements for Human Subject Protection Training

Based on PIRB's policies and procedures, the Project Protocol Review Form requires investigators to verify that each member of the research team has successfully completed training in human research subject protection. Your institution may have additional training requirements, please check with your institutional official.

PIRB accepts training completed in a variety of formats (e.g., online modules, live seminars, college courses, self-study texts that provide CEU or CME credit) and from a variety of sources (e.g., government entities, non-profit institutions, professional organizations, and commercial businesses). However, it is PIRB policy that all investigators, key personnel, OHRO staff, and PIRB board members complete the following educational requirements:

• Completion of CITI course
• Copy of current Curriculum vitae (preferably within 2 years of research protocol and signed/dated) If you would like a sample or working template, one is provided Here for your use.

If you have questions regarding PIRB training requirements, please contact any member of the OHRO staff at: 309-680-8630.

Nurses seeking consent to obtain Cord Blood Donation for Research Purposes must complete the following:

1) Review Human Subjects Research Participation slide.

2) Complete Nurse Test

3) Return test to the OHRO office, ATTN: Mindy Reeter

&NOTE: This education series does not satisfy requirements for new Principal

                              Investigators wishing to engage in new research.

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

This page last updated on 7/17/07

Click for IRB Home



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

This page last updated on 04/06/06