Resumen
This document specifies the general requirements for, and offers guidance on, processes, programs and procedures for development, validation and routine control of aseptic processing of health care products.
This document includes requirements and guidance relative to the overall topic of aseptic processing.
Specific requirements and guidance on various specialized processes and methods related to sterilizing filtration, lyophilization, clean-in place (CIP) technologies, sterilization in place (SIP) and isolator systems are given in the other parts of the ISO 13408 series.
Informaciones generales
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Estado: PublicadoFecha de publicación: 2023-08Etapa: Norma Internacional publicada [60.60]
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Edición: 3Número de páginas: 72
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Comité Técnico :ISO/TC 198ICS :11.080.01
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Ciclo de vida
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Anteriormente
RetiradaISO 13408-1:2008
RetiradaISO 13408-1:2008/Amd 1:2013
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Ahora