2008 Seminars


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Patricia Kerby, MPA
Office of Human Subjects Protection
Compliance Office Links and Resources
Title: Certificate in Clinical Research
Date Presented: February 13, 2008  
Discussant: Elizabeth Webb, M.A.  
Title: ICH GCP Guidelines when
Documenting Study Events
Date Presented: March 12, 2008  
Discussant: Derita Bran, RN, CCRC  
Title: Biosafety for the
Clinical Researcher
Date Presented: April 9, 2008  
Discussant: Francine Rogers, M.S., ALM, RBP, CBSP, SM  
Title: Introduction to iMedRIS
Date Presented: May 14, 2008
Discussant: Cameron Barclay, Kim Prachniak, and Tricia Page  
Title: Research under HIPAA
Date Presented: June 11, 2008  
Discussant: Alisa Firehock and
Attorney Robert Wilson
Title: Speed Bumps in the
Clinical Trial
Contracting Process
Date Presented: July 9, 2008
Discussant: Alexis Tutor, J.D.
Title: The Informed Consent Zone  
Date Presented: September 10, 2008 Reflections Informed Consent
Discussant: Patricia Kerby, MPA PowerPoint - The Informed Consent Zone
Title: FDA Warning Letters Reflections FDA Warning Letters: Don’t Make the Same Mistakes
Date Presented: October 8, 2008 FDA Sample Forms
Discussant: Neysa Rhoads, RN, CCRC PowerPoint-FDA Warning Sign
Title: The Ethics of Placebo Controls in Randomized Clinical Trials Reflections Header
Date Presented: November 13, 2008 PowerPoint-Placebo Controlled Trials
Discussant: Terrence F. Ackerman, Ph.D.  

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