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Home » Getting DSMBs, IRBs In Sync With Adverse-Event Reporting
Getting DSMBs, IRBs In Sync With Adverse-Event Reporting
May 3, 2006
Sponsors confronted with a clinical trial adverse event (AE) must also be prepared for scrutiny regarding how they selected and set up their data safety monitoring board (DSMB), expert Mark Barnes warned at an April 24 FDAnews audioconference.