Waiver to Informed Consent Process in Research Planned for Emergency Settings- PRO119   

 

 

Abstract: 
This procedure lists responsibilities of the investigator, IRB, OIRB, and sponsor for waiver to the informed consent process in research planned for emergency settings.

Effective Date: 3/30/2007

 

Review/Revised Date: 2/7/2020

 

Category: Research

 

Policy Owner: Vice President for Research

Policy Contact:

 

   
 
 
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