May 16
UPDATE: Evaluating Plastic Syringes Made in China for Potential Device Failures: FDA Safety Communication
Medical Devices
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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Medical Devices
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Medical Devices
Since its inception in 1994, OWH has been at the forefront of ensuring that the unique health needs of women are met through a multifaceted approach.
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.
FDA MedWatch Safety Information
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