Severity of a COVID-19 illness could be determined by examining autoantibodies in the nasal cavity, allowing more personalized treatment protocols. Severe COVID-19 can be life-threatening for patients ...
The FDA has granted emergency approval use for a coronavirus test that can be conducted by patients at their homes. The FDA re-issued emergency use approval for the Pixel by LabCorp COVID-19 home ...
Each week, the University and its testing partners process over 10,000 samples, most of which are collected on campus, then shipped beyond the state to laboratories in Massachusetts. Despite the ...
On April 21, the Food and Drug Administration awarded its first authorization for a nasal self-swab home test, made by LabCorp. The agency had previously issued warnings to consumers about “fraudulent ...
An Army-Harvard team of expert scientists have been performing “specialized testing” of industry built swab prototypes to ensure that new, alternative designs meet the requisite performance and ...
Rite Aid is expanding its drive-thru Covid-19 testing locations with seven new sites. The company announced Saturday additional site locations will be opening on April 20 in New York, New Jersey, ...
SAN DIEGO, May 29, 2024 /PRNewswire/ -- Biolabs International LLC announced earlier in May an exclusive partnership with Watmind USA ™; the manufacturer of the acclaimed SpeedySwab ™ Covid-19 Antigen ...
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