Clinical Research Operations Program: General Reporting Requirements

Nov 29, 2017 (Wed) | 12:15 PM -1:45 PM
Li Ka Shing Center, LK120 : Stanford, CA

Learn which types of information (adverse events, regulatory non-compliance, unanticipated problems, protocol deviations) need to be reported to whom (sponsor, IRB, FDA) and when (emergently vs. routinely). Registration required. Enroll here:

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

Contact: Jessica P Meyer | 6504986140 |


  • Jennifer Brown, RN Director, Clinical Research Quality

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