You may have noticed that more and more people are testing positive for COVID-19 after using a rapid test to swab their throats. The trend took off on Twitter this past week, and unlike most of the ...

WALTHAM, Mass. & WATERTOWN, Mass.--(BUSINESS WIRE)--Rhinostics Inc. and Nexus Medical Labs recently received Emergency Use Authorization (EUA) from the US Food and Drug Administration (FDA) for a ...

Biosensors are being used as a tool for detecting the presence of SARS-CoV-2 in patients and diagnosing COVID-19. Early and rapid detection of the disease will help manage the outbreak by curbing the ...

Anyone who has had a COVID-19 PCR test done knows the drill — a swab up the nose and then the tester pops the swab into a plastic bag and off it goes. That’s when the hard work begins of determining ...

Surveillance remains a critical strategy for reducing the impacts of coronavirus disease 2019 (COVID-19) while the transmission of severe acute respiratory syndrome coronavirus 2 (SAR-CoV-2) continues ...

In a recent study posted to the medRxiv* preprint server, researchers developed a high-throughput, rapid antigen severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein detection ...

QIAGEN N.V. QGEN recently announced the receipt of emergency use authorization (EUA) from the FDA for its QIAreach SARS CoV-2 Antigen Test. This rapid portable test is designed to address the ...

Please provide your email address to receive an email when new articles are posted on . The BD MAX Respiratory Viral Panel detected and differentiated between influenza A and B respiratory syncytial ...

HAUPPAUGE, N.Y., Dec. 06, 2021 (GLOBE NEWSWIRE) -- Chembio Diagnostics, Inc. (Nasdaq: CEMI), a leading point-of-care diagnostics company focused on infectious diseases, today announced that it has ...