The FDA's sentinel initiative-A comprehensive approach to medical product surveillance

In May 2008, the Department of Health and Human Services announced the launch of the Sentinel Initiative by the US Food and Drug Administration (FDA) to create the Sentinel System, a national electronic system for medical product safety surveillance. This system complements existing FDA surveillance...

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Veröffentlicht in:	Clinical pharmacology and therapeutics 2016-03, Vol.99 (3), p.265-268
Hauptverfasser:	Ball, R, Robb, M, Anderson, SA, Dal Pan, G
Format:	Artikel
Sprache:	eng
Schlagworte:	Adverse Drug Reaction Reporting Systems Equipment and Supplies - adverse effects Equipment and Supplies - standards Humans Pharmacovigilance Product Surveillance, Postmarketing United States United States Food and Drug Administration - legislation & jurisprudence
Online-Zugang:	Volltext
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