Clinical Trial Investigator Series: What You Should Know About Monitoring and Auditing (Quality Control and Quality Assurance)

Date: Tuesday, April 17, 2012 Time: 3:00 PM - 4:00 PM
Location: Bondurant Hall, Room 3074
Seats available: 4 Register/Cancel by: 4/17/2012 9:00 AM


Description:

The purpose of this series is to provide education on how to successfully conduct clinical trials of drugs and devices. The intended audience is faculty, residents, or fellows who are, or aspire to be, clinical trial investigators. This module focuses on how to set up a Q/A program for investigator-initiated trials, and what to expect during external audits.


Presenters: 

Marie Rape, Regulatory Core Associate Director, TraCS Institute
Mary O’Dwyer, Associate Director of Regulatory Affairs & Administrative Services, Clinical Protocol Office, Lineberger Comprehensive Cancer Center


Prerequisites:


Registration:

  • An Onyen is required for registration. If you do not have one, please contact the Center for Faculty Excellence at 919.966.1289 to be added to the registration list.

 

 

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