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VERSION:2.0
PRODID:-//UIC
BEGIN:VEVENT
UID:2026040508492520250328T12000020250328T13000069d2221555eae@uic.edu
CATEGORIES:MEETING
STATUS:TENTATIVE
DTSTAMP:20250303T094520
DTSTART:20250328T120000
DTEND:20250328T130000
SUMMARY:After IRB Approval…Keeping Your Study Compliant
DESCRIPTION:  Description:   What investigators need to know and how to prepare when their study is selected for monitoring. Review and discussion of the Clinical & Human Subject Research Compliance program?s purpose and process to assist investigators in maintaining study compliance.  Speaker:   Erin Vidra, MS, CHRC  Director, Clinical & Human Subject Research Compliance  Office of Vice Chancellor for Research    \n    Clinical Research Investigators Seminar Series (CRISS): This training seminar series is intended to provide faculty and other investigators with information and skills needed to conduct clinical research at UIC at all stages of a study?s lifecycle.    \n      Register  | Event post: https://ahs.uic.edu/inside-ahs/events?page_id=25702
LOCATION:    Select 
CLASS:PRIVATE
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