100 IRB Institutional Review Board (IRB) Review of Human Subject Research Protocols or FDA-Regulated Activities Involving Human Participants

    Revision Date: 
    March 20, 2018
    Responsible Official: 
    Institutional Review Board Executive Chair
    Responsible Office: 
    Office of Research Administration
    PDF icon 100 IRB Institutional Review Board (IRB) Review of Human Subject Research Protocols or FDA-Regulated Activities Involving (189.05KB)