Clinical Research Operations Program: The Informed Consent Process

Aug 16, 2017 (Wed) | 9:00 AM -11:00 AM
HRP, T138B : Palo Alto, CA

This class will describe the informed consent process and answer the following questions: What is informed consent? Why is it important? Who is involved in the process? Where and when does informed consent take place? And finally, how should the process be conducted? Additional topics to be discussed include electronic consent, short form consent, and the re-consent process. Best practices and case studies will also be reviewed.

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

Contact: Kiera Larsen, RN | (650) 721-4027 |


  • Kiera Larsen, RN Education Program Manager, SCCR

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