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

Jan 19 () - Pharmaceutical company Boehringer Ingelheim said on Monday the U. Food and Drug ​Administration had approved its ...

Jan 28 (Reuters) - Regenxbio said on Wednesday the U.S. Food and Drug Administration has placed a clinical hold on two of its experimental gene therapy programs for rare childhood diseases, sending ...

The U.S. Food and Drug Administration (FDA) is celebrating a historic milestone in 2026, marking 120 years of national ...

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. - ...

In a series of high-impact moves, the FDA is reshaping how it approves and regulates drugs, including accelerating reviews, revising vaccine standards and simplifying biosimilar development.

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 ...

Dec 12 (Reuters) - Leaders at the U.S. Food and Drug Administration have pressed internally for reviewers to speed up their evaluation ‌of Eli Lilly's experimental weight‑loss pill, after the company ...

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 ...

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 scrutiny following ...