Feb 12 (Reuters) - The U.S. Food and Drug Administration said on Thursday it has approved labeling changes to six menopause ...

Disc Medicine said on Friday the U.S. Food and Drug Administration has declined to approve its drug to treat a rare genetic disorder.

Feb 10 (Reuters) - The U.S. Food and Drug Administration on Tuesday launched a broad review of a long-used synthetic ...

The PreCheck programme, first unveiled in June 2025, aims to speed up drug facility construction.

On Feb. 10, pharmaceutical company Moderna announced that the FDA Center for Biologics Evaluation and Research (CBER) had refused to review its application to market an investigational mRNA-based flu ...

This reassessment of BHA is the first in a larger post-market review program for food chemicals started by the Joe Biden ...

The U.S. Food and Drug Administration said a television advertisement for Novo Nordisk's weight-loss pill is "false or misleading", according to a letter dated 5.

Add Yahoo as a preferred source to see more of our stories on Google. One study estimated that in their first year of use, Covid-19 vaccinations averted almost 20 million deaths around the world. - ...

Dec 9 (Reuters) - U.S. health regulators informed senior executives at Merck, Sanofi and AstraZeneca last week that their ‌approved protective RSV treatments for infants would face fresh safety ...

The FDA launched PreCheck pilot program to strengthen U.S. drug supply chain by improving regulatory predictability.

The US Food and Drug Administration intends to put a “black box” warning on Covid-19 vaccines, according to two people familiar with the agency’s plans, the latest move by President Donald Trump’s ...