New IRB Training on Regulatory Documentation – April 2022
Ethical and effective conduct of human research requires careful documentation and record retention. Sign up for a special training session to learn all about regulatory requirements and best practices for regulatory documentation in human research!
Sessions will be held virtually using Zoom, on the following dates:
- Wednesday, April 13, 9am-10am ET (Register here)
- Friday, April 15, noon-1pm ET (Register here)
- Monday, April 18, 4pm-5pm ET (Register here)
Join the IRB to learn all about regulatory requirements and best practices for regulatory documentation in human research. Representatives from the Human Research Protection Program (HRPP) Post-Approval Monitoring and Quality Improvement Program (PAMQuIP) will discuss this topic, and introduce attendees to the Study Conduct Toolkit – a collection of resources that will help study teams ensure they are compliant with regulatory requirements for documentation and record retention.
Following this session, attendees will be able to:
- Articulate regulatory requirements for documentation and record retention in human research
- Develop a regulatory binder for a human research study
- Utilize the study conduct toolkit to engage in best practices for regulatory documentation