New York Post may be compensated and/or receive an affiliate commission if you buy through our links. Featured pricing is subject to change. COVID-19 — it’s still a thing, which means it’s always a ...

WHO said the decision builds on earlier emergency approvals and reflects the continued need for affordable, fast COVID-19 testing even after the pandemic’s emergency phase.

Artificial intelligence-focused healthcare technology company Gauss partnered with Cellex, a biotech company specializing in point-of-care diagnostic testing, to create the first rapid COVID-19 ...

On 17 December 2025, the World Health Organization (WHO) announced the prequalification of two rapid antigen diagnostic tests ...

The FDA has extended the shelf life for some COVID-19 tests. Now that allergy season is here, many are finding themselves with symptoms asking: Is it allergies or a cold? COVID? Something else? Since ...

The Food and Drug Administration is making it easier for people to simultaneously test themselves for COVID-19 and the flu at home. The agency this week authorized the Healgen Scientific's Rapid Check ...

NAAT tests, including PCR tests, are more likely to detect the virus, and are considered the “gold standard” for COVID-19 tests. Samples are usually taken in a health-care setting and sent to a lab ...

The Becton Dickinson lab-free COVID-19 test was already in use in the US, and the company is now in talks with European governments.

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 ...

"I would still say that distancing and outdoor air are your best friends," one leading public health expert told Insider.

The FDA has issued emergency authorizations to 12 antibody tests for the virus. As federal officials gradually begin reopening the country, expanded testing is central to the conversation. Until now, ...