483
Ursa Brown-GlabermanUrsa Brown-Glaberman – FDA 483, Dec 19, 2025
Record Details
An FDA inspection of Ursa Brown-Glaberman in Albuquerque, NM, identified a significant issue related to clinical trial conduct. The firm failed to promptly report serious adverse events (SAEs) to the study sponsor for multiple participants, indicating a lapse in adherence to protocol requirements for timely safety reporting.
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ID · 6a5ea1a7-b5b6-4265-8f28-45bafe2b0fc2
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