This course will provide recent updates from to the Human Research Protection Program (HRPP)/Institutional Review Board (IRB) from representatives from the Research Compliance Office (RCO).   This course will include where to locate “What’s New” and an overview of single IRB (sIRB) processes and upcoming resources.

By attending this workshop, you will:

• Recognize the required items for submitting a new IRB protocol application to the IRB for review
• Identify when sIRB is needed and follow local sIRB process
• Locate the most current consent templates, including Spanish-translated consent templates, and recent revisions

Learn more about the Stanford Clinical Research Operations Program.