483
Robert M. Haws, M.D.Robert M. Haws, M.D. – FDA 483, Sep 4, 2020
Record Details
An FDA inspection of Robert M. Haws, M.D. in Marshfield, WI, identified a significant deviation from an investigational plan. The clinical investigator failed to adhere to the study protocol for dose escalation in a clinical trial, leading to potential subject safety concerns. This non-compliance involved multiple subjects and specific protocol sections related to study design and drug dose adjustments.
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ID · 906bb9d6-60f7-4348-9277-bdaa950d6681
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