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FDA Launches Postmarket Chemical Review Program to Ensure Food Safety

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Program includes review of existing chemicals, developing final, systematic process for postmarket review

FDA Gives Full OK to Novavax COVID Shot for High-Risk Groups

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By I. Edwards HealthDay Reporter MONDAY, May 19, 2025 (HealthDay News) — The U.S. Food and Drug Administration (FDA) has granted full approval to Novavax’s...

HHS, FDA Begin ‘Operation Stork Speed’ to Improve Quality of Infant Formula

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Agencies say significant progress has already been made; input has been requested from the public

FDA Approves At-Home Cervical Cancer Test for Women Ages 25 to 65

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By I. Edwards HealthDay Reporter MONDAY, May 12, 2025 (HealthDay News) — Women now have a new way to check their risk for cervical cancer...

Dr. Vinay Prasad to Head FDA Vaccine, Biologics Division

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By I. Edwards HealthDay Reporter WEDNESDAY, May 7, 2025 (HealthDay News) — The U.S. Food and Drug Administration (FDA) has chosen Dr. Vinay Prasad, a...

Top FDA Inspection Official to Retire Amid Staff Frustration

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By I. Edwards HealthDay Reporter WEDNESDAY, May 7, 2025 (HealthDay News) — The official in charge of federal food and drug safety inspections will retire...

COVID Boosters Might Not Be Updated for Next Season, FDA Commissioner Says

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By Dennis Thompson HealthDay Reporter TUESDAY, May 6, 2025 (HealthDay News) -- The head of the U.S. Food and Drug Administration (FDA) reiterated Tuesday that...

FDA Commissioner: No Major Reorganization, Just Smart Reforms

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By I. Edwards HealthDay Reporter THURSDAY, May 1, 2025 (HealthDay News) — Dr. Marty Makary had just finished his last surgery at Johns Hopkins when...

FDA Approves Zevaskyn for Rare, Genetic Skin Disorder

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Zevaskyn is the first and only autologous cell-based gene therapy for recessive dystrophic epidermolysis bullosa

FDA Warns of Unapproved Hair-Loss Product Linked to Side Effects

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By I. Edwards HealthDay Reporter THURSDAY, April 24, 2025 (HealthDay News) — A quick spray of medication might seem like an easy way to get...