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DIN EN ISO 13408-2

Aseptic processing of health care products - Part 2: Filtration (ISO 13408-2:2003)

inactive
Organization: DIN
Publication Date: 1 September 2011
Status: inactive
Page Count: 22
ICS Code (Pharmaceutics in general): 11.120.01
ICS Code (Sterilization and disinfection in general): 11.080.01

Document History

DIN EN ISO 13408-2
June 1, 2018
Aseptic processing of health care products - Part 2: Sterilizing filtration (ISO 13408-2:2018)
This document specifies requirements for sterilizing filtration as part of aseptic processing of health care products conducted in accordance with ISO 13408-1. It also offers guidance to filter users...
DIN EN ISO 13408-2
April 1, 2017
Aseptic processing of health care products - Part 2: Sterilizing filtration (ISO/DIS 13408-2:2017); German and English version prEN ISO 13408-2:2017
A description is not available for this item.
DIN EN ISO 13408-2
September 1, 2011
Aseptic processing of health care products - Part 2: Filtration (ISO 13408-2:2003)
A description is not available for this item.

References

This document is referenced by:
DIN EN ISO 14534 - Ophthalmic optics - Contact lenses and contact lens care products - Fundamental requirements (ISO 14534:2011)
Published by DIN on August 1, 2015
This International Standard specifies safety and performance requirements for contact lenses, contact lens care products, and other accessories for contact lenses. This International Standard does...
This document is referenced by:
DIN EN 556-2 - Sterilisation von Medizinprodukten - Anforderungen an Medizinprodukte, die als "STERIL" gekennzeichnet werden - Teil 2: Anforderungen an aseptisch hergestellte Medizinprodukte; Deutsche Fassung EN 556-2:2015
Published by DIN on November 1, 2015
Diese Europäische Norm legt die Anforderungen an ein aseptisch hergestelltes Medizinprodukt fest, das als „STERIL“ gekennzeichnet wird. ANMERKUNG Für die Anwendung der EU-Richtlinie(n) für...
This document is referenced by:
DIN EN ISO 13408-1 - Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013)
Published by DIN on December 1, 2015
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...

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