Resumen
This document specifies procedures for the generation of medical device extracts for chemical characterization testing to support toxicological risk assessment. It supports the activities of EN ISO 10993-18:2020 that depend on chemical analysis of device extracts for chemical characterization.
Informaciones generales
-
Estado: En desarrolloEtapa: Nuevo proyecto aprobado [10.99]
-
Edición: 1
-
Comité Técnico :ISO/TC 194
- RSS actualizaciones