Using UV light technology, Tamarack's TruActive process eliminates pathogens while preserving the enzymes, proteins and ...

Phathom Pharmaceuticals, Inc. announced that the FDA has approved its Citizen Petition, recognizing 10 years of New Chemical Entity exclusivity for its medication VOQUEZNA® (vonoprazan ...

Commissioner Marty Makary was quick to pat FDA developers on the back for completing the project "ahead of schedule and under budget," touting the administration as a leader among federal agencies ...

For those unfamiliar with the medication, the FDA approved mifepristone about a quarter of a century ago, to be used as part of a two-step process to terminate unwanted pregnancies up to 10 weeks.

Cultivated seafood has cruised to become a reality. US startup Wildtype has received regulatory approval from the US Food and Drug Administration (FDA) to sell its sushi-grade cultivated salmon in the ...

Soon after Yutrepia (treprostinil) was approved by the U.S. Food and Drug Administration (FDA) to treat some forms of pulmonary hypertension, the therapy’s maker, Liquidia, scheduled its first ...

The U.S. Food and Drug Administration (FDA) has approved the first artificial intelligence (AI) tool to predict breast cancer risk. The authorization was confirmed by digital health tech company ...

On May, 28, the FDA marked the tomato recall affecting three states as Class I, meaning there is a risk of "serious adverse health consequences or death." The tomato recall, initiated by ...

A new Food and Drug Administration AI tool that could speed up reviews and approvals of medical devices such as pacemakers and insulin pumps is struggling with simple tasks, according to two ...

Clairity, Inc., a digital health innovator advancing AI-driven healthcare solutions, has received U.S. Food and Drug Administration (FDA) De Novo authorization for CLAIRITY BREAST, a novel ...