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Introduction/WIC Description PDF Print E-mail

Welcome to the Wisconsin Institutional Review Board (IRB) Consortium (WIC) website!  The primary purpose of WIC is to facilitate collaboration among member institutions' Institutional Review Boards (IRBs) in order to provide more effective and efficient oversight of multi-site human subject research protocols in Wisconsin and reduce costs and duplication of effort among the Member institutions and affiliated investigators. The Consortium has established one agreement that allows any member institution to serve as the IRB of record for another and eliminates the need to draft individual, study-specific IRB authorization agreements for each study reviewed.


WIC is in its development/pilot phase and as such is limited to the following participants:

  • Aurora Health Care IRB, Milwaukee
  • Marshfield Clinic IRB, Marshfield
  • Medical College of Wisconsin IRB, Milwaukee
  • University of Wisconsin-Madison Health Sciences IRB, Madison

 

If you are an investigator from one of the institutions listed above who is collaborating on a project with an investigator from another one of the participating institutions, your project is eligible for review through the WIC process.  See Directions for Submission for more details.

 
Directions for Requesting Review PDF Print E-mail
Written by Administrator   
Tuesday, 22 June 2010 07:32

Wisconsin IRB Consortium

Directions for Requesting Review of New Studies

 

Important information before you request WIC review

·         WIC deferral is not automatic. You will be notified of a decision.

·         Do not begin human subject activities until IRB approval is obtained.

·         A request must involve collaborators from two or more WIC institutions.

·         You may be subject to auditing by the WIC IRB of record or one of the collaborating sites.

·         The lead investigator is responsible for communication between collaborating sites and assuring that the correct protocol is being followed.

·         Do not submit any IRB applications to any site until you receive a response from WIC.

·         Any WIC member’s IRB may at any time immediately assume IRB review and oversight responsibility. You will be notified if this should happen.

·         WIC will not accept studies involving prisoners.

 

Directions for submission

 

1.      Download and complete the WIC Project Description and Review Request Form <link>.

2.      Submit the WIC Request Form to your local IRB using the link on the WIC website. A copy of the protocol, draft consent documents, and institution-specific approvals must be included with the form. If no protocol exists, one should be developed using the protocol format described on the WIC website. The Request Form must clearly specify what study activities will occur at each site.

3.      Do not submit an IRB application until you receive a response from WIC.

4.       You will be notified by WIC whether or not your request has been approved.

5.      Submit an IRB application as directed by WIC.

6.      The IRB of record will notify the PI of IRB determinations.  

7.      The WIC PI (PI at institution serving as IRB of record) must notify collaborating investigators of IRB determinations.

 

 

Last Updated on Tuesday, 22 June 2010 07:46