fda-approval is the sole category represented across all 1 tracked stories. FDA is the most frequent co-covered peer, appearing in 1 of the 1 tracked story. At 7, the average consequence score sits above the same-window beat average of 6.
Figures are computed live from our source-verified story record
— see our methodology for how impact and
sentiment are derived.
What the coverage shows about NG-TEST Candida auris
fda-approval is the sole category represented across all 1 tracked stories. FDA is the most frequent co-covered peer, appearing in 1 of the 1 tracked story. At 7, the average consequence score sits above the same-window beat average of 6. Source depth averages 2 original sources per story, versus 2.4 across the same-window beat baseline. NG-TEST Candida auris appears in 1 tracked Biotech story from February 19, 2026.
Stories tracked
1
Sources per story
2
Computed from the 1 stories linked to this entity, with beat comparisons drawn from all 27 Biotech stories published in the same date window. Shares are omitted below five stories and comparisons below a twenty-story baseline.
Coverage cohort
Appears alongside
Other entities that clear the same relevance threshold in stories also covering NG-TEST Candida auris. Shared-story counts are live from our verified record — not editorial picks.
NG Biotech and partner Hardy Diagnostics have received FDA Breakthrough Device Designation for two rapid diagnostic tests targeting Candida auris and Acinetobacter baumannii. These assays aim to provide near-instant identification of high-priority antimicrobial-resistant pathogens to improve hospital infection control.
NG-TEST Candida auris is linked from 1 story on this site, each scored at or above our 35% relevance threshold — see how these pages are built.
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