The Food and Drug Administration Thursday granted full approval for Moderna's COVID-19 vaccine, Spikevax, in children aged 6 ...

Moderna, Inc. (MRNA) on Thursday announced that the U.S. Food and Drug Administration (FDA) has fully approved its COVID-19 ...

SILVER SPRING, MD — The FDA gives full approval for Moderna’s COVID-19 vaccine in children aged 6 months through 11 years who ...

Fresh off of the heels of a shakeup at the CDC over vaccine recommendations, many Americans still question the necessity and safety of COVID-19 vaccines for young children.

While an emergency use authorization may be the speediest way for public health officials to begin a vaccination campaign, it may not end up shaving that much time off of a more traditional route to ...

SPEAR® LEP secures EU emergency use authorization from fourth country ahead of anticipated full regulatory approvalKalamazoo, Michigan, July 08, 2025 (GLOBE NEWSWIRE) -- Portugal has granted emergency ...

What is an emergency use authorization? An emergency use authorization is a tool that the FDA uses to strengthen the nation’s response to public health emergencies such as COVID-19.

The first COVID-19 vaccine was distributed under an Emergency Use Authorization. More than seven months later, actual approval hasn’t been granted.

Emergency use authorization can be granted when a vaccine meets certain standards during a time when there is extreme risk to public health.

Until recently, you may have never heard the term “Emergency Use Authorization.” These words entered the lexicon as people around the world anxiously read updates about the COVID-19 pandemic ...

Emergency use authorization can be granted when a vaccine meets certain standards during a time when there is extreme risk to public health.