This informative session explores some of the tools of the clinical research trade including data extraction and adverse event reporting.
The presenter reviewed adverse events and serious adverse event reporting, medical record data extraction and collection, and review SAE-related medical records with existing medical history.
Upon completion of this continuing education program, participants should be able to:
Define adverse events.
Define serious adverse events
Reviewing medical records with baseline medical history.
Speaker:
Pranali Wandile, MS, CCRP, Clinical Research Manager, South Carolina Clinical Research LLC
