Please provide your email address to receive an email when new articles are posted on . Labcorp has received FDA emergency use authorization for its Mpox PCR Test Home Collection Kit. This test is now ...

The Food and Drug Administration has set March 8 as the end of its emergency use authorization (EUA) for Paxlovid for adult patients, the agency has said this week. The medication is given to those ...

Transitioning COVID-19 tests from emergency use authorization to the traditional pre-market pathway has long been a goal for the FDA. “Today’s authorization is the first at-home COVID-19 test granted ...

Please provide your email address to receive an email when new articles are posted on . The updated COVID-19 vaccine targets the currently circulating Omicron variant JN.1 strain of the virus. The ...

The Food and Drug Administration has withdrawn emergency use authorization for AstraZeneca’s Covid-19 antibody cocktail Evusheld as the treatment is not expected to neutralize the currently dominant ...

The COVID-19 public health emergency’s end doesn’t affect the U.S. Food and Drug Administration’s authority to issue new emergency use authorizations related to the novel coronavirus. That’s because a ...

Physicians can order the test for patients who will receive the kit directly for sample collection at home. The Food and Drug Administration (FDA) has granted Emergency Use Authorization (EUA) to ...

SAN DIEGO--(BUSINESS WIRE)--Cue Health (“Cue”) (Nasdaq: HLTH), a healthcare technology company, today announced it has received Emergency Use Authorization (EUA) from the United States Food and Drug ...