The U.S. Food and Drug Administration has declined to approve PTC Therapeutics' drug to treat a rare genetic disorder with ...

A series of panels convened by the Food and Drug Administration is raising concerns that the agency is skirting federal rules ...

Emergency use authorizations will give farmers and veterinarians quicker access to resources to protect animals and the food ...

The Food and Drug Administration (FDA) became authorized Tuesday to allow the use of animal drugs to treat or prevent infestations caused by the New World screwworm, a flesh-eating parasite that has ...

The initiative is a response to a Trump administration order to speed the construction of the type of new drug factories many ...

There are currently no FDA-approved drugs for screwworm in the United States. The emergency use authorization allows the use ...

Families concerned about color additives in school lunches, at grocery stores and at fast-food counters can now reference a ...

More than 5,000 pounds of cheese products made by Middlefield Original Cheese Co‑op are being voluntarily recalled after the ...

The U.S. Department of Health and Human Services (HHS) issued a declaration on Aug. 19 allowing the U.S. Food and Drug Administration (FDA) to issue Emergency Use Authorizations (EUAs) for animal ...

The FDA said in letters to five sunscreen makers that they are not authorized to market sunscreen sold in mousse or whipped form.

Animal studies suggest that some food additives, such as artificial colorants and sweeteners, emulsifiers, and antimicrobial ...

The U.S. Food and Drug Administration has denied approval for PTC Therapeutics' oral medication for a rare genetic disorder ...