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Adverse Event/Serious Adverse Event Management - Mar. 20th, 2024 is a Course

Adverse Event/Serious Adverse Event Management - Mar. 20th, 2024



Full course description

Learn about prompt and proper management of adverse events (AEs) and serious AEs (SAEs) encountered in human subject research with drugs, how they must be documented and tracked, and, under certain conditions reported to Sponsors, regulatory agencies, and IRBs. Put this learning to practice with case studies.

Learning Objectives

At the conclusion of this class, you will be able to:

  • Identify adverse events and adverse events classification
  • Explain the Stakeholder responsibilities
  • Recognize the Information flow
  • Understand the Reporting timelines
  • Discuss Case studies

Audience: Research coordinators, nurses, faculty, staff, and post-doctoral scholars working on clinical research projects at Stanford University. 


Session Date: Wednesday March 20th, 2024

Time:               9:00 - 11:00 AM

Location:         Virtual Meeting. This class will be held LIVE on the date above. 


Clinical Research Professional Competency DomainClinical Trials Operations (GCPs)
Clinical Research Operations Program: Elective

This is an elective seminar in the Clinical Research Operations Program. Please complete the evaluation at the end of the seminar.


 (Links to an external site.

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