Full course description
This class will provide the audience with an overview of when use of a Single IRB is required and the Single IRB (sIRB) process at Stanford University. We will review Single IRB requirements, the steps for creating the sIRB eProtocol application, discuss the documents to include in the sIRB application, the informed consent language requirements when relying on an external IRB, and the local requirements after setting up the reliance.
By attending this workshop, you will:
- - Understand when use of Single IRB is Required
- - Understand the IRB reliance process
- - Know what documents are required for submission of the sIRB eProtocol application
- Understand the roles and responsibilities of Stanford study team and Stanford IRB
Session Date: Thursday May 8th, 2025
Time: 9:30 - 11:00 am
Location: Virtual Seminar. Enroll, return to the course website to obtain the zoom link. This class will be held LIVE on the date above.
This is an elective course in the Clinical Research Operations Program. Please complete the evaluation at the end of the seminar.
Clinical Research Professional Competency Domain: Study and Site Management
Audience: Research coordinators, nurses, faculty, staff and post-doctoral scholars working on clinical research projects at Stanford University.