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 

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Session Date: Wednesday, Apr. 26, 2023
Time: 12:00 - 1:30 pm
Location: Virtual Seminar. Enroll, return to the course website to obtain the zoom link. This class will be held LIVE on the date above.

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This is an elective course in the Clinical Research Operations Program. Please complete the  evaluation within 30 days post-class date.

Clinical Research Professional Competency Domain: Study and Site Management

Audience: Faculty, Fellows, Residents, Nurses and Staff working on research projects at Stanford University.