UNE-EN ISO 13408-6:2011
Superseded
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005)
Amended by
Available format(s)
Hardcopy , PDF
Superseded date
16-02-2022
Superseded by
Published date
28-12-2011
Publisher
Important note : Users cannot be edited or removed once added to your Multi user PDF.| Committee |
CTN 111
|
| DevelopmentNote |
Supersedes UNE EN 13824. (01/2012)
|
| DocumentType |
Standard
|
| Pages |
28
|
| PublisherName |
Asociacion Espanola de Normalizacion
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| ISO 13408-6:2005 | Identical |
| EN ISO 13408-6:2011 | Identical |
| ISO 13408-4:2005 | Aseptic processing of health care products — Part 4: Clean-in-place technologies |
| IEST RP CC006.2 : 1997 | TESTING CLEANROOMS |
| ISO 10648-1:1997 | Containment enclosures — Part 1: Design principles |
| ISO 13408-1:2008 | Aseptic processing of health care products — Part 1: General requirements |
| ISO/TS 11139:2006 | Sterilization of health care products Vocabulary |
| ISO 14644-7:2004 | Cleanrooms and associated controlled environments — Part 7: Separative devices (clean air hoods, gloveboxes, isolators and mini-environments) |
| ISO 14644-1:2015 | Cleanrooms and associated controlled environments Part 1: Classification of air cleanliness by particle concentration |
| ISO 9001:2015 | Quality management systems — Requirements |
| ISO 10648-2:1994 | Containment enclosures — Part 2: Classification according to leak tightness and associated checking methods |
| ISO 14971:2007 | Medical devices Application of risk management to medical devices |
| ISO/IEC 90003:2014 | Software engineering Guidelines for the application of ISO 9001:2008 to computer software |
| ISO 13408-5:2006 | Aseptic processing of health care products Part 5: Sterilization in place |
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