The Food and Drugs Authority (FDA) on Wednesday urged street food vendors to refrain from reselling leftover food to reduce the incidence of food poisoning and promote public safety. It said the ...

Call or text 988 or chat at 988lifeline.org. The U.S. Food and Drug Administration is warning the public about a drug rising in popularity, commonly referred to as "gas station heroin." ...

The FDA rejected Axsome's AXS-14 fibromyalgia, prompting a new trial and pushing the expected drug launch to 2028.

Axsome Therapeutics received a refusal-to-file letter from the Food and Drug Administration for its new drug application for its fibromyalgia drug AXS-14.

New Jersey-based AACE Pharmaceuticals has been slammed in an FDA warning letter citing significant violations by its contract manufacturer Brassica Pharma, including substandard sanitary ...

(WIFR) - The U.S. Food and Drug Administration recently approved the first-ever blood test to help confirm Alzheimer’s disease, thanks to data from the Wisconsin Alzheimer’s Institute.

The FDA expects that randomized, controlled trial data on clinical outcomes will be needed before COVID-19 vaccines can be approved for patients who are 6 months to 64 years of age and do not have ...

The system is fully repositionable and available in multiple sizes. Abbott announced the FDA approved its transcatheter mitral valve replacement system for patients with severe mitral annular ...

Sonji Collins requested a Special Use Permit (SUP) from the City of Rockford to operate a food pantry in a building she owns. Wall Street Journal Shatters Core Trump Fantasy In Editorial Urging ...

There are about 3,000 permit applications pending with the regulator, FDA Director Maria Cecilia C. Matienzo told the panel. The delays in the processing of FDA permit applications have a “big effect” ...

recommending the FDA permit updated COVID-19 boosters for people 65 and older and those with at least one high-risk health condition. For healthy individuals under 65, vaccine manufacturers would ...

Irvine Labs Inc. ("Irvine Labs"), an FDA-compliant and DEA-registered facility in California, United States has successfully received its Controlled Substances Import Permit for psilocybin raw ...