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EU Regulators Back First Combined COVID-19 and Flu mRNA Shot for Adults 50 and Over

A European Commission decision now determines EU authorization, after which Member States will set pricing and rollout.

FDA Delays Two Drugs in National Priority Voucher Program After Safety, Efficacy Flags

Hawley Pressures FDA Chief as Anti‑Abortion Groups Demand Firing Over Reported Mifepristone Review Delay

Missouri, Kansas and Idaho Sue to Block FDA’s New Generic Mifepristone Approval, Curb Mail-Order Access

FDA Approves Second Generic Mifepristone as White House Cites Legal Obligation

FDA Escalates Crackdown on Drug Ads, Moves to Close ‘Adequate Provision’ Loophole