Sarepta halts US shipments of Duchenne therapy, bowing to FDA

Sarepta bows to FDA pressure, pulls Duchenne drug from market

FDA, Stop Foodborne Illness Food Safety Culture Webinar Series Returns

FDA names former pharmaceutical exec to oversee drug program

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Siemens Healthineers Receives FDA Clearance for Two Multifunctional Imaging Platforms

July 21, 2025 — Siemens Healthineers has received Food and Drug Administration clearance for two multifunctional imaging platforms for radiography and fluoroscopy, or real-time 2D imaging: the remote-controlled Luminos Q.namix R and the Luminos Q.namix T …

MAJOR RECALL OF POWER STICK DEODORANTS ANNOUNCED BY FDA, AFFECTING OVER 67,000 CASES NATIONWIDE

FDA taps biotech industry veteran as RFK Jr.'s top drug regulator 

FILE PHOTO: The headquarters of the U.S. Food and Drug Administration (FDA) is seen in Silver Spring, Maryland November 4, 2009.  Jason Reed | Reuters The Food and Drug Administration said Monday it has appointed former biotech executive George Tidmarsh as …

FDA Approves Prefilled Syringe Presentation for Shingles Vaccine

FDA Commissioner names George Tidmarsh as new CDER director

FDA Commissioner Marty Makary has named George Francis Tidmarsh, M.D., Ph.D., the new Director of the Center for Drug Evaluation and Research, succeeding acting director Jacqueline Corrigan-Curay. Effective immediately, Tidmarsh, a former biopharma …

FDA Clears New Radiography/Fluoroscopy Systems from Siemens Healthineers

The Food and Drug Administration (FDA) has granted 510(k) clearance for the Luminos Q.namix R and Luminos Q.namix T radiography/fluoroscopy systems that may enhance efficiency and reduce radiation exposure for specialized and complex examinations. …