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 ...

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 ...

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 ...

In a recent study posted to the medRxiv* preprint server, researchers identified that morning-collected nasal and saliva samples yielded better detection of severe acute respiratory syndrome ...

Adding a throat swab specimen to a nasal specimen significantly increased sensitivity of COVID-19 rapid antigen tests, whether self-collected or collected by a healthcare worker, a randomized clinical ...

Basel, 6 December 2021 - Roche (SIX: RO, ROG; OTCQX: RHHBY) today announced its plans to launch the SARS-CoV-2 & Flu A/B Rapid Antigen Test for professional use in markets accepting the CE Mark by 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 ...