
Aseptic Processing Of Health Care Products - Part 1: General Requirements (Iso 13408-1:2008, Including Amd 1:2013)
出版:Comite Europeen de Normalisation

專家解讀視頻
Describes 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.
Supersedes EN 13824. (07/2011)
ONORM EN ISO 13408-1:2015 - Identical
NF EN ISO 13408-1:2016 - Identical
UNI EN ISO 13408-1:2015 - Identical
SN EN ISO 13408-1:2015 - Identical
PN EN ISO 13408-1:2015 - Identical
NEN EN ISO 13408-1:2015 - Identical
SS EN ISO 13408-1 Ed. 2 (2015) - Identical
NBN EN ISO 13408-1:2011 - Identical
I.S. EN ISO 13408-1:2015 - Identical
ONORM EN ISO 13408-1:2014 - Identical
DIN EN ISO 13408-1 (2013-08) - Identical
DS EN ISO 13408-1:2011 - Identical
UNI EN ISO 13408-1:2013 - Identical
BS EN ISO 13408-1:2011+A1:2013 - Identical
UNE EN ISO 13408-1:2011 - Identical
SN EN ISO 13408-1:2011 - Identical
NS EN ISO 13408-1:2011 - Identical
NF EN ISO 13408-1:2011 - Identical