Stanford Clinical Research Operations Program: The Stanford IRB Process

Jan 25, 2017 (Wed) | 12:15 PM -1:15 PM
269 Campus Drive : Stanford, CA

This class will provide the audience with an overview of human subjects research, the Institutional Review Board (IRB) at Stanford, and a broad discussion of the regulatory framework as well as Stanford specific guidance and policies. We’ll define what is and what is not human subjects research and what type of protocol should be submitted the using eProtocol (eP) system. The overall process: initial submission, modifications, continuing reviews, and reporting to the IRB will be reviewed. Types of documents that need to be submitted and elements that must be included in the informed consent as well as different ways informed consent can be obtained will be discussed.

Department:  Spectrum: Center for Translational and Clinical Research and Education

Contact: Jessica P. Meyer, Spectrum Education Coordinator | 650-498-6140 | jpmeyer@stanford.edu

Presenter(s):

  • Lisa Denney, MPH, CIP Associate Director for Program Development, Stanford Researc

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