Resumen
This document specifies the whole manufacturing process of Chinese materia medica products by defining a set of domain constraints of sanctioned characteristics, each composed of a relationship and an applicable categorial structure. It includes three process categories: processing, extracting and preparation.
This document is not applicable to Japanese traditional KAMPO medicinal products.
Informaciones generales
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Estado: PublicadoFecha de publicación: 2020-01Etapa: Norma Internacional confirmada [90.93]
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Edición: 1Número de páginas: 8
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Comité Técnico :ISO/TC 215ICS :35.240.80
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