DOCR training: Adverse Events

This course will help participants define adverse events and unanticipated problems, and it will help investigators identify study team member responsibilities in recognizing these events. It will also define reporting responsibilities of study team members to the FDA, funding agencies, and the DUHS IRB.

External Info

http://docr.som.duke.edu/education/register-trainings

Type of Opportunity

  • Course

Area of Interest

  • Clinical research methods