We offer a series of "CTSA" instructor-led courses on all aspects of conducting human subjects research (HSR), as well as a series on budgeting for clinical trials. These courses are offered throughout the year and repeat regularly. You can register for these courses via Skillsoft (Registration Instructions).

If you need more personalized training for your group, we’re happy to help! Please contact us to begin customizing your training.

CTSA10: Reporting to the IRB - Requirements After Initial Approval

| 01:00 PM - 02:00 PM
Contact :
Clinical Research Support Center
Email :
clinicalresearchsupportcenter@ucdenver.edu
Phone :
(303) 724-1111
This class will be offered remotely via Zoom. Register for remote access here: https://ucdenver.zoom.us/meeting/register/tJ0tceGvrDwuGtfuGpwHh3-77ubb9ZxyBgfL 

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