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Negocios · 8/9/20141 min de lectura
Postmarketing Safety Reports for Human Drug and Biological Products; Electronic Submission Requirements; Corrections
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Resumen
The Food and Drug Administration (FDA) is correcting a document entitled "Postmarketing Safety Reports for Human Drug and Biological Products; Electronic Submission Requirements; Correction" that appeared in the Federal Register of August 14, 2014 (79 FR 47655). The document published without the required RIN number and in the Notice category. This document corrects those errors.
Idioma original de la fuente: Federal Register — Food and Drug AdministrationAbrir el comunicado original →