2007-2008 IRB Training Program Schedule

Please Note: Meeting dates, times and locations are subject to change, so please check back regularly for updates.

Date	Session Title	Time	Location
December 12, 2007	"The IRB: Who We Are and What We Do"	10:00-11:00 AM	J103
January 16, 2008	"Initial Study Submissions to the IRB"	10:00-11:00 AM	J103
February 13, 2008	"IRB Stipulations and Response to Stipulations"	10:00-11:00 AM	J103
March 19, 2008	"Informed Consent"	10:00-11:00 AM	J103
April 16, 2008	"Continuing Review and Completion Reporting"	10:00-11:00 AM	M115
May 14, 2008	“Adverse Event Reporting and Follow-Up”	10:00-11:00 AM	M115
June 18, 2008	“IRB Reporting: Changes and Updates”	10:00-11:00 AM	J103
July 16, 2008	“Vulnerable Populations”	10:00-11:00 AM	M115
August 20, 2008	“Using a Commercial IRB”	10:00-11:00 AM	M115
September 17, 2008	“FDA and OHRP Regulations – Compared and Contrasted”	10:00-11:00 AM	J103
October 15, 2008	"Interactive Mock IRB Meeting"	10:00-11:00 AM	J103
November 12, 2008	“On-Site Research Review and Setting up an Internal Audit Program”	10:00-11:00 AM	J103

We are working on having CEUs for credentialing approved so that we can offer certificates to you. Details will follow as they become available.

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