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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
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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 |
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