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.

November 10, 2009	“Consenting Subjects: Different Approaches with Panel Discussion”   Presented by:  Amy Deem, RN; Wajeeh Bajwa, PhD; Pam Schreck, RN, MSN; Sherri Mizrahy, RN, MSN, CPON; Meiko Dunn, MHA, CSCS
November 19, 2009 12-4 PM	“IRB Boot Camp”   Presented by:  Terry Lemesh, IRB Education Coordinator
December 8, 2009	“Documenting the Informed Consent Process”   Presented by: Ray Moseley, PhD., Associate Professor, Bioethics, Law and Medical Professionalism

January 12, 2010	“Developing a Clinical SOP Manual”   Presented by: Wajeeh Bajwa, PhD, Director Office of Regulatory Affairs and Licensing, CTSI
February 9, 2010	“Social-Behavioral Research, Collecting Data via On-Line Sites”   Presented by: Ira Fischler, PhD., Professor Emeritus, Department of Psychology

 

 

 

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.