Jul 09
Maquiladora Miniara S.A. de C.V. Issues Voluntary Nationwide Recall of Shine and Clean Hand Sanitizer and Due to Potential Presence of Undeclared Methanol (Wood Alcohol)
Drugs
FDA Commissioner Dr. Robert M. Califf discusses nutrition and offers a peek at some new packaging label prototypes.
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Health professionals, consumers and patients can voluntarily report observed or suspected adverse events for human medical products to FDA. Voluntary reporting can help FDA identify unknown risk for approved medical products.
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Drugs
Aug 20
Medical Devices
Aug 30
Drugs
The 50th biosimilar approval milestone also reflects our strategic approach to biosimilars, as outlined in the FDA’s Biosimilars Action Plan.
I recently had the privilege of official travel to the European Union with our global affairs team.
I recently had the privilege of official travel to the U.K. with our global affairs team.
FDA MedWatch Safety Information
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