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Negocios · 6/10/20001 min de lectura

Regulations Requiring Manufacturers to Assess the Safety and Effectiveness of New Drugs and Biological Products in Pediatric Patients; Technical Amendment

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Resumen

The Food and Drug Administration (FDA) is amending the biologics regulations to reincorporate a regulation that was inadvertently omitted. This action is being taken to improve the accuracy of the regulations.

Idioma original de la fuente: Federal Register — Food and Drug AdministrationAbrir el comunicado original →