Collaboration underscores MethodSense’s role in accelerating market access and regulatory confidence for advanced ...
Looser regulations around consumer-grade wearable devices could be a "path to ROI" for health systems—or a "double-edged ...
Medical Device Network on MSN
KORU Medical receives FDA clearance for FreedomEDGE infusion system
Rystiggo is administered weekly, 3ml to 6ml over 15 to 30 minutes for six weeks.
Discover how small US egg farms are driving FDA registrations, growing 3.5x faster than large producers and transforming the ...
As the quick-service restaurant industry digests the recent announcement that the U.S. Food and Drug Administration will ...
Ulanqab Kema’s growth is underpinned by a multifaceted strategic advantage. Its location in Ulanqab, Inner Mongolia, provides ...
How the industry can break the larger goal of full supply chain traceability into manageable, achievable steps ...
In an era where AI-driven drug discovery accelerates candidate generation faster than traditional systems can evaluate them, ...
Medical Device Network on MSN
FDA clears Cepheid’s Xpert GI Panel for pathogen detection
The Xpert GI Panel identifies pathogens directly from stool specimens collected in Cary-Blair transport media.
For much of the past decade, drug shortages in the United States were treated as episodic disruptions. In 2024, that framing ...
The U.S. FDA’s October 2025 draft guidance for quality management system information in premarket filings may have struck some observers as an example of regulatory overreach, given the robust ...
FDA approvals, trial progress and early commercial momentum put several ASX healthcare companies in a strong position heading ...
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