The Food and Drug Administration on Monday issued a guidance for the tobacco industry entitled Validation and Verification of ...

AccurKardia has gained the US Food and Drug Administration's (FDA) breakthrough device designation for its AI-powered ‘AK+ ...

Blue Ridge Beef is recalling 1,350 pounds of its raw cat food sold across the Northeast and mid-Atlantic after the product ...

The change was prompted by postmarketing observational studies that suggest an increased risk of GBS within 42 days of ...

WATERTOWN, Mass., Jan. 08, 2025 (GLOBE NEWSWIRE) -- Vigil Neuroscience, Inc. (Nasdaq: VIGL), a clinical-stage biotechnology ...

Text message-based programming and the drug varenicline were the only 2 strategies that were shown to be effective for quitting vaping.

Investigational new drug (IND) applications for initiating first-in-human studies for ZW220 and ZW251 in solid tumors anticipated in 2025IND applications for initiating first-in-human studies for ZW20 ...

“The proposed rule, Tobacco Product Standard for Nicotine Level of Certain Tobacco Products, is displaying in the Office of ...

A database of medical device reports shows a patient enrolled in a Varipulse study had a stroke shortly after treatment. Read ...

LUMRYZ, is an extended-release sodium oxybate medication approved by the FDA on May 1, 2023, as the first and only once-at-bedtime treatment for cataplexy or excessive daytime sleepiness (EDS) in ...

New York-based global healthcare data technology company H1 announced in a press release on January 8 the acquisition of ...

The temporary halt to investigate reported neurovascular events comes two months after Johnson & Johnson won FDA approval for ...