The European Union should allow drug prices to rise to U.S. levels in order to attract investment, the bosses of two European ...

The U.S. Food and Drug Administration approved the use of Sanofi and Regeneron's blockbuster drug Dupixent for patients with ...

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The US Food and Drug Administration announced Thursday that it will be phasing out a requirement that monoclonal antibodies and other drugs be tested on animals, saying in a news release that ...

Get Instant Summarized Text (Gist) The FDA's approval of high-risk medical devices has reached a 10-year low, attributed to significant workforce reductions. Despite an increase in pending ...

U.S. Food and Drug Administration approvals of life-changing, high-risk medical devices reportedly slowed to a 10-year low for the January to March period, as recent layoffs have reportedly had ...

On March 26, 2025, the Company announced that the U.S. Food and Drug Administration (FDA) issued an Approvable Letter regarding the Company's Pre-Market Approval (PMA) application for the Genio ...

In this first installment of "Exit Interviews," MedPage Today editor-in-chief Jeremy Faust, MD, sits down with two-time FDA Commissioner Robert Califf, MD, to discuss what it was like running a ...

As President Donald Trump’s massive overhaul of federal agencies continues, several former FDA officials spoke about the potential ramifications for drug reviews and provided a look inside curre ...

The delay dovetails with moves by Republican lawmakers in at least 7 states to ban or limit mRNA vaccines. HealthDay News — The US Food and Drug Administration (FDA) has delayed the full ...