EVANSTON, Ill.--(BUSINESS WIRE)--Minute Molecular Diagnostics today announced that the U.S. Food and Drug Administration (FDA) granted an Emergency Use Authorization (EUA) for its rapid DASH ...

FDA-authorized test for home use is the most affordable PCR-quality rapid test on the market and at least 50 times more sensitive than leading rapid antigen tests Detect’s FDA authorized PCR-quality ...

BOSTON & OXFORD, England & CAMBRIDGE, England & TORONTO--(BUSINESS WIRE)--Global molecular diagnostics innovator Sense Biodetection (Sense) today announced it has entered into a strategic agreement ...

COVID-19 and its latest Omicron strains continue to cause infections across the country as well as globally. Serology (blood) and molecular tests are the two most commonly used methods for rapid COVID ...

Since the start of the pandemic, the FDA has issued emergency use authorizations to a whopping 444 diagnostic tests and sample collection devices to detect the COVID-19 virus. In recent months, ...

A new program from eMed and the NIH offers free tests and treatments, and you don't even need to leave your home.

A Covid-19 antigen self-test kit shows a positive case on January 13, 2022 in Madrid. - Spain today agreed to cap the cost of Covid antigen tests at just under three euros after the government came ...

The public will no longer need a prescription or a visit to a health provider to take take a combined COVID and flu test at home. The U.S. Food and Drug Administration on Thursday announced it has ...

No, you didn’t set your clocks too far back for the end of daylight saving time. This week, the FDA granted its first full, bona fide clearance to an over-the-counter home antigen test for COVID-19, ...

Determining whether you have a cold, the flu or Covid-19 might be getting a little easier soon. On Friday, the U.S. Food and Drug Administration authorized the first over-the-counter combination test ...