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FDA Releases Report of the Number of Foreign Drug Facilities Inspections in...

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Many Drug Companies have yet to Self-Identify with the FDA

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U.S. Marshals Seize Unapproved Drug Products Being Marketed As Supplements

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FDA to Require Pharmaceutical Applications to be Submitted Electronically

On May 5, 2015, the U.S. Food and Drug Administration (FDA) published a final guidance document requiring certain pharmaceutical product applications to be submitted in Electronic Common Technical...

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