Skip To Content
General and IRB Reporting Requirements- June 26, 2024 is a Course

General and IRB Reporting Requirements- June 26, 2024



Full course description

The seminar will discuss what information is reportable (ie. adverse events, regulatory non-compliance, protocol deviations, annual reports, new information) as well as to whom the information is reportable, and the specifics surrounding required IRB reporting by providing guidance on when and how to submit unanticipated problems, noncompliance, and other IRB reportable events.


By attending this workshop, you will:
- Identify what should be reported to whom and via which mechanisms
- Recognize the difference between routine reports and emergent or prompt reports
- Know what documents are required for submission of a prompt report to the IRB
- Understand the role of the IRB and external reporting requirements


Course open to all faculty, fellows/residents, staff working on clinical research projects at Stanford.


Date:            Wednesday June 26th, 2024
Time:           12:15 - 1:45 pm
Location:    Virtual / Live Webcast


Note: The zoom link will be sent to enrolled participants the day of the class. After enrolling, return to the course website to download the course materials and find the zoom information.  


Certificate Program – Core Class
Core Competency: Clinical Trials Operations

Sign up for this course today!