Reporting Adverse Events

Unanticipated problems or serious adverse events involving risk to human subjects must be reported to the IRB immediately.  An Event Reporting Form detailing the problem(s) should be submitted to following:

UNC Charlotte IRB

Angelica Martins, Interim Director, Office of Research Compliance, 300 Cameron Hall

Sherry Loyd, Associate Director, Office of Research Compliance, 320 Cameron Hall