UF - Institutional Review Boards

Links to our IRB websites:
IRB Home
Link to IRB-01 Gainesville Health Science Center
Link to IRB-02 UF Campus/Non-Medical
Link to IRB-03 Jacksonville Health Science Center
Link to IRB-04 Western IRB (WIRB)

Training Site Links
Training Home
Required Reading
DHHS Training Requirements
Educational Events
Additional Training
Newsletter Archives
Liaison Support
Educational Needs Assessment
Other Resources

 

IRB Educational Events - Calendar of Ongoing Training Programs

Unless otherwise noted, all training programs listed below will be held in the McKnight Brain Institute room
LG-110A (ground floor) from 12:00 PM to 1:30 PM. Please e-mail Terry Lemesh or call 392-7875 to register.

March 11, 2008

"IRB Forms” (Terry Lemesh) AND  
"VA Human Subjects Research: Forms and the Submittal Process" (Jaime Passaro, VA Human Subjects Research Coordinator)

April 8, 2008 Informed Consent” (Linda Fallon) AND
Costs to Consent” (Deborah Townsend, Clinical Trials Compliance)
May 13, 2008: Quality Assurance Audits” Shelly Ogiste

 

 

Missed a lecture? Link to previous PowerPoint presentations

HIPAA Training:

  • HIPAA & Research Training: required for all Principal Investigators and strongly recommended for other research staff. Click here for more info.
  • HIPAA Training: visit the UF Privacy Office web site for more information.

 


 
University of Florida Last updated February 27, 2008 15:11