CTN webinar: IRB and regulatory documentation.

This 1-hour session will focus on Institutional Review Board (IRB) requirements and oversight in the conduct of research trials, particularly in the CTN, as well as the requirements for regulatory document management at the site, Node compliance, and regulatory document obligations to the sponsor.

Objectives include:

• Identifying critical aspects of IRB oversight and compliance
• Determining appropriate regulatory documentation practices
• Explaining roles and responsibilities involved in reporting progress to regulatory bodies.

Target Audience: Everyone is welcome! You do not have to be a CTN member to register for this webinar.

Presented by Emily Dorer, University of Cincinnati, OV Node, and Ro Shauna Rothwell, PhD, Wayne State University.

Additional Resources:

• Download slides (pdf)