Resumen
ISO 27593-2:2011 seeks to create a standardized framework for international regulatory reporting and information sharing by providing a common set of data elements and a messaging format for transmission of ICSRs for adverse drug reactions (ADR), adverse events (AE), infections, and incidents that can occur upon the administration of one or more human pharmaceutical products to a patient, regardless of source and destination.
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Informaciones generales
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Estado: PublicadoFecha de publicación: 2011-12
Versión corregida (en): 2012-10Etapa: Norma Internacional confirmada [90.93] -
Edición: 1Número de páginas: 585
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Comité Técnico :ISO/TC 215ICS :35.240.80
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