FDA 483 - Beasley E. Robert, MD - July 21, 2025

Robert E. Beasley, MD, a clinical investigator in Fort Lauderdale, FL, was cited for failing to conduct an investigation according to the investigational plan. The inspection revealed significant delays in reporting serious adverse events (SAEs) to the sponsor. Multiple SAEs were reported months, and in some cases over a year, after the firm became aware of them.