NEW YORK -- Moderna is seeking emergency use authorization from the US Food and Drug Administration for its Covid-19 vaccine for children 6 months through 5 years of age, the company said Thursday.

The FDA has issued an emergency use authorization for lotilaner chewable tablets (Credelio Cat; Elanco Animal Health) for treating New World screwworm (NWS) infestations in cats and kittens. Credelio ...

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 ...

In October 2025, the FDA announced that it issued an emergency use authorization for otilaner chewable tablets (Credelio Cat; ...

The news of several promising COVID-19 vaccines over the past few weeks has been very exciting, but so far, none have ...

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 ...

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 ...

On Sunday, Aug. 23, the U.S. Food and Drug Administration announced an emergency use authorization of convalescent plasma therapy to help treat COVID-19. An emergency use authorization from the FDA ...

BURLINGTON, North Carolina -- LabCorp has received emergency use authorization from the Food and Drug Administration for its Pixel at home coronavirus test kit. The COVID-19 At Home Test Kit allows ...

The FDA Advisory Committee approved Pfizer for emergency use authorization for its Covid-19 vaccine on Thursday evening, paving the way for an immediate nationwide rollout aimed at stopping the ...

Oct 21 (Reuters) - A panel of independent experts to the U.S. health regulator will decide on the nature of clinical trials that coronavirus vaccines should go through after receiving U.S. emergency ...

The experimental drug remdesivir has been approved to treat hospitalized patients with severe Covid-19, the US Food and Drug Administration said in a letter on Friday. The experimental drug remdesivir ...