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.

OU Medicine, University of Oklahoma Health Sciences Center and Oklahoma Medical Research Foundation File for FDA Emergency Use Authorization for COVID-19 Detection Test Utilizing ...

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 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 ...

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 ...

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 ...

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 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 ...

Pfizer announced Friday that it would submit a request to the FDA Friday for its COVID-19 vaccine to be granted Emergency Use Authorization. Earlier this week, Pfizer said that a final analysis of ...

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 ...