Resumen
ISO/TS 22224:2009 encompasses the electronic reporting of adverse reactions caused by drugs for human uses. Thus, other businesses relating to adverse events caused by blood transfusion, medical devices and veterinary drugs are excluded from the scope of ISO/TS 22224:2009.
Informaciones generales
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Estado: RetiradaFecha de publicación: 2009-10Etapa: Retirada de la Norma Internacional [95.99]
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Edición: 1Número de páginas: 11
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Comité Técnico :ISO/TC 215ICS :35.240.80
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