The Food and Drug Administration on Wednesday authorized the first rapid coronavirus test that doesn’t need any special computer equipment to get results. The 15-minute test from Abbott Laboratories ...

More than two years after the World Health Organization (WHO) declared an end to the emergency phase of the Covid-19 pandemic, the virus continues to circulate globally. While current data suggest ...

Add Yahoo as a preferred source to see more of our stories on Google. Over-the-counter multiplex tests for more than one illness may soon come to a pharmacy near you. Paco Burgada/iStock via Getty ...

US Food and Drug Administration (FDA) has granted emergency use authorization (EUA) to the first COVID-19 diagnostic test that can be used to provide rapid results at-home. The newly authorized Lucira ...

Select independently determines what we cover and recommend. When you buy through our links, we may earn a commission. Learn more. At-home Covid tests can diagnose infection and are in stock now ...

The CLINITEST Rapid COVID-19 Antigen Self-Test has received FDA EUA for unsupervised self-testing for the SARS-CoV-2 virus by individuals age 14 and older (or adult-collected samples from individuals ...

Point of Care Facilities Authorized to Use GenBody’s Nasopharyngeal and Anterior Nasal Swab Test Kits to Test People Without Symptoms JURUPA VALLEY, California--(BUSINESS WIRE)--GenBody America is ...

You probably have a cabinet full of rapid COVID-19 tests you’ve accumulated. The expiration dates have come closer and closer, with some tests even reaching them. The Food and Drug Administration, ...

BRUSSELS, Nov 18 (Reuters) - The European Commission recommended on Wednesday the use of rapid COVID-19 antigen tests mostly on people already showing symptoms because it said the kits were deemed ...