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- VertigoDx receives FDA 510(k) clearance for its portable SmartVertigo diagnostic systemThe U.S. Food and Drug Administration has issued a 510(k) clearance for VertigoDx's portable vertigo assessment tool, allowing it to be marketed in the United States. The system, called SmartVerti…
- American Biotech Innovation Alliance urges Congress to prioritize US leadership in biopharmaThe American Biotech Innovation Alliance, formed in May, appeared on Capitol Hill on September 30, 2026 to address lawmakers. The group argued that maintaining U.S. dominance in biopharma requires…