Event Detail

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CTSA10: Reporting to the IRB - Requirements After Initial Approval

| 01:00 PM - 02:00 PM
Clinical Research Support Center

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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