Troubleshooting Informed Consent

The Office of Responsible Research Practices and the Center for Clinical and Translational Science are offering a workshop on common informed consent screening and IRB review findings, and consent issues that arise during ongoing research projects.  The session will:

• Identify common submission screening questions
• Examine IRB-required modifications related to the consent process
• Discuss common post-approval monitoring findings
• Review best practices and available resources

While the session will be tailored to medical researchers, anyone preparing IRB submissions is welcome.