483
Kamran Qureshi, M.D.Kamran Qureshi, M.D. – FDA 483, Apr 28, 2023
Record Details
An FDA inspection of Kamran Qureshi, M.D. in Saint Louis, MO, identified a significant issue regarding the conduct of an investigation. The clinical investigator failed to maintain control and accountability for study drugs, specifically eleven missing study kits. This indicates a serious lapse in adherence to the investigational plan and regulatory requirements for drug management.
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