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Research Education > Activities and Resources > Navigating the IRB and Investigator Responsibilities

Session 3 Topic: Obtaining Informed Consent
This Session Will Be Offered:
Wednesday, November 18, 2009
Time and Location:
11:30 a.m.-1:00 p.m.
Rebecca Sealy East 4.302/4.304

Session 1: Overview of the Institutional Review Board
Session 2: Getting Started - Initial Submission and Ongoing Research Review
Session 3: Obtaining Informed Consent

 

Topics Discussed:
  • Review Requirements for Informed Consent Process
    - Documenting Informed Consent
    - Form
    - Who Can Obtain Consent
    - Who Can Sign the Form
    - Witnesses
  • Acceptable Methods for Retention of Signed Consents
Video Presentation:
"The Consent Zone" (30 minutes - Optional)

Speaker:
Dr. Michele Carter, Associate Professor, Institute for the Medical Humanities and
Research Subject Advocate, General Clinical Research Center

 

 
 
   
 


     
 

Last Modified: 10/01/2009
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