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.