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 government approval. Is it the right tool to use to start COVID-19 vaccination campaigns?

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 FDA issued an emergency use authorization to drug-maker Lilly for bamlanivimab, a monoclonal antibody that mimics the immune system’s response to infection with the virus that causes COVID-19.

WASHINGTON — Two viewers reached out to the Verify team about the FDA’s Emergency Use Authorization -- known as an EUA -- and how it differs from full FDA "approval." During Verify'a "Ask the ...

Moderna, Inc. (MRNA) on Thursday announced that the U.S. Food and Drug Administration (FDA) has fully approved its COVID-19 vaccine Spikevax in children aged six months through 11 years who are at increased risk for the disease.

Since then, federal immigration agents have intensified operations throughout Southern California, acting on Trump’s directive for ICE to use “all in their power” to execute what he has described as the largest mass deportation campaign in American history, Newsweek noted.

Provider organizations have answered the Department of Health and Human Services’ (HHS’) call for deregulation suggestions with their policy change wish lists tackling topics from prior authorizati | Hospital and clinician associations' responses to HHS' deregulation inquiry featured plenty of recurring administrative pain points and broad calls for flexibility in other areas like staffing,

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 use authorization (EUA) for Vestaron’s groundbreaking bioinsecticide SPEAR® LEP,

The FDA this week fully approved Moderna’s COVID-19 vaccine for children aged 6 months to 11 years but limited the approval to those with at least one underlying condition that puts them at risk for severe disease.

The Centers for Medicare and Medicaid Services (CMS) will implement prior authorization requirements for certain traditional fee-for-service Medicare services in six states starting next year.

Portugal has granted emergency use authorization (EUA) for Vestaron’s groundbreaking bioinsecticide SPEAR® LEP, enabling farmers to protect tomato crops from devastating infestations