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Clinical Research Operations Program: General Reporting RequirementsNov 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: http://bit.ly/CTR-0110 Department: Spectrum: Center for Translational and Clinical Research and Education Contact: Jessica P Meyer | 6504986140 | jpmeyer@stanford.edu Presenter(s):
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