
Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013)
出版:Standardiserings-Kommissionen I Sverige

专家解读视频
This part of ISO 13408 specifies the general requirements for, and offers guidance on, processes, programmes and procedures for development, validation and routine control of the manufacturing process for aseptically-processed health care products.
ISO 13408-1 : 2008(R2017) - Identical
ISO 13408-1 : 2008(R2017) - Identical
EN ISO 13408-1 : 2015 - Identical