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DTSTART:20061101T020000
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UID:1369289660671.mdanderson.org
ORGANIZER;CN=Leola Griffin:MAILTO:opreducation@mdanderson.org
DTSTAMP:20130523T011420
DTSTART;TZID=Central Standard Time:20120910T120000
DTEND;TZID=Central Standard Time:20120910T130000
SUMMARY:Office of Protocol Research (OPR) Brown Bag Session: IRB Policy for Investigators on Reporting Unanticipated Adverse Events for Drugs and Devices
LOCATION:AT&T Auditorium, Main Building, Floor 2 (B2.4750)
DESCRIPTION:\n1.      Purpose of the Presentation? To inform clinical research faculty and staff of the revised IRB policy for Investigators on Reporting Unanticipated Events for Drugs and Devices. \n2.      Which regulations or institutional policies are relevant to discussion? 21 CFR 812.150(a) (1)  21 CFR 812.3 (s) \n3.      Who will it impact (eg. researchers, admin staff, sponsors, etc)? All clinical research faculty and staff. \n4.      When will the changes be implemented? October 1, 2012.\n\nLocation   : AT&T Auditorium, Main Building, Floor 2 (B2.4750)\nFormat     : All Employee Meeting\nContact    : Leola Griffin - opreducation@mdanderson.org\n\nEvent URL  : http://www3.mdanderson.org/calendar/event/Office_of_Protocol_Research_OPR_Brown_Bag_Session_IRB_Policy_for_Investigators_on_Reporting_Unanticipated_Adverse_Events_for_Drugs_and_Devices_17895.html
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