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The CU Anschutz Medical Campus leadership is closely monitoring the transitions to better understand the impacts on our research community.

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Event Detail


Learners may register for sessions by first signing into the Denver | Anschutz portal with their CU credentials.


glasses sitting on an open book

CTSA10: Reporting to the IRB - Requirements After Initial Approval

| 01:00 PM - 02:00 PM
Contact:
Clinical Research Support Center
Email:
clinicalresearchsupportcenter@ucdenver.edu

To register in advance via Skillsoft, click the button below, and sign into the "Denver | Anschutz" option with your CU credentials when prompted.

This training will review the reporting responsibilities of the PI once the study has been initially approved by COMIRB. It will include how to submit unanticipated problems, amendments, and continuing review requirements.

Content Level: Intermediate

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