For Health Professionals

For Health Professionals

Medical product safety information, adverse event/problem reporting and more.

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How to Report Adverse Events to FDA MedWatch

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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FDA Expert Commentary and Interview Series on Medscape

FDA Updates Regulations on Mammography – June 2019

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