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Regulatory Environment

DCOC IRB Administrators: Study Start to Finish

This DCOC functional group, IRB Administrators, discuss their role in ISPCTN studies, explain how the role changes during the course of the study, and, explain how the work as liaisons between cIRB and relying sites.  *ECHO ISPCTN Core Curriculum Module

External Training Resources for the Engagement in Human Subjects Research

Valuable materials to assist with getting you started with engaging in human subjects research.

What's so Special About FDA Trials?

This webinar covers the regulations and guidelines ECHO ISPCTN will need to follow in FDA trials that differ from prior studies and the roles and responsibilities of principal investigators and other research team members in FDA trials. *ECHO ISPCTN Core Curriculum Module