FDA Clears Hologic’s Aptima SARS-CoV-2 Assay
Hologic, Inc. has received FDA 510(k) clearance for its Aptima SARS-CoV-2 assay, initially authorized for emergency use in 2020.
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Multiplex Test for SARS-CoV-2, Flu A, Flu B, and RSV Receives 510(k) Clearance
Thermo Fisher Scientific has received FDA 510(k) clearance for its Applied Biosystems TaqPath COVID-19, Flu A, Flu B, RSV Select Panel, a real-time PCR multiplex test.
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Gastroenterologist Access Lacking for Many Americans
Nearly 50 million Americans, particularly in rural areas, face barriers to seeing a gastroenterologist, needing to travel at least 25 miles.
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HealthTrackRx Advances the Fight Against Antibiotic Resistance
HealthTrackRx’s new anthem video underscores its mission to combat antibiotic resistance by delivering next-morning results.
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BD Plans to Separate Biosciences and Diagnostic Solutions Business
Summary:BD (Becton, Dickinson and Company) announced its plan to separate its Biosciences and...
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