2009 Archived Seminars

Patricia Kerby, MPA
Office of Human Subjects Protection
Compliance Office Links and Resources

Title:
How to Survive a FDA Inspection
Date Presented:
January 14, 2009
Discussant:
Patricia Kerby
 
 
 
 
Title:
Informed Consent: Ethical Concepts and Practical Realities
Date Presented:
March 19, 2009
Discussants:
Dr. Terrence Ackerman - Informed Consent: Ethical Concepts
Dr. Haavi Morreim
- Informed Consent: Digging Into the Realities
Dr. Sydney Ornduff
- Informed Consent: Digging Out of the Realities
 
 
 
 
 
Handouts (pdf)
Title:
Legal Issues of Medical Research
Date Presented:
April 8, 2009
Discussant:
Carol Schwab, J.D. LL.M
 
use RealPlayer to view the video
Title:
"Strategies to Increase African American Participation in Clinical Research"
Date Presented:
May 14, 2009
Discussant:
Mona Wicks, PhD, RN
 
 
Title:
"The Research Coordinator Toolbox: What to Include"
Date Presented:
June 11, 2009
Discussant:
Derita Bran, RN, CCRC
 
 
   
 
This presentation does not constitute legal advice. The views expressed are the presenter's own and do not necessarily express the views of UT Medical Group, Inc.
Legal Issues in Clinical Research
Date Presented:
September 10, 2009
Title:
"You've been Warned…Everyday Occurrences that Landed your Colleagues with a Warning Letter from the FDA"
Discussant:
Laura Cummins, JD
 
Title:
"Medicare Coverage and Billing Requirements for Clinical Trials"
Discussant:
Carol Schwab, JD, L.L.M
 
Title:
"Authoritative Writings, Evidenced-Based Medicine and the Rules of Evidence"
Discussant:
David Cook, JD
 
Date Presented:
October 8, 2009
Title:
"Introduction to Collaborative Institutional Training Initiative (CITI)"
Discussant:
Patricia Kerby, MPA, Office of Human Subjects Protection Compliance Officer