UNLIMITED FREE
ACCESS TO THE WORLD'S BEST IDEAS

SUBMIT
Already a GlobalSpec user? Log in.

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

Customize Your GlobalSpec Experience

Select Your Free Newsletters

Industry Newsletters

Select Your Free Product Alerts

Finish!
Privacy Policy

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

DIN EN ISO 13408-4

Aseptic processing of health care products - Part 4: Clean-in-place technologies (ISO 13408-4:2005)

active, Most Current
Organization: DIN
Publication Date: 1 September 2011
Status: active
Page Count: 25
ICS Code (Sterilization and disinfection in general): 11.080.01

Document History

DIN EN ISO 13408-4
September 1, 2011
Aseptic processing of health care products - Part 4: Clean-in-place technologies (ISO 13408-4:2005)
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 - Aseptische Herstellung von Produkten fuer die Gesundheitsfuersorge - Teil 1: Allgemeine Anforderungen (ISO 13408-1:2008, einschliesslich Amd 1:2013); Deutsche Fassung EN ISO 13408-1:2015
Published by DIN on December 1, 2015
Der vorliegende Teil von ISO 13408 legt die allgemeinen Anforderungen an Verfahren, Programme und Verfahrensweisen zur Entwicklung, Validierung und Routinekontrolle des Herstellungsverfahrens 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...
This document is referenced by:
DIN EN ISO 13408-6 - Aseptische Herstellung von Produkten fuer die Gesundheitsfuersorge - Teil 6: Isolatorensysteme (ISO 13408-6:2005 + Amd 1:2013); Deutsche Fassung EN ISO 13408-6:2011 + A1:2013
Published by DIN on July 1, 2013
Der vorliegende Teil von ISO 13408 legt die Anforderungen an Isolatorensysteme fest, die bei der aseptischen Herstellung eingesetzt werden, und stellt einen Leitfaden zur Qualifizierung,...
This document is referenced by:
DIN EN ISO 13408-6 - Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005 + Amd 1:2013) (includes Amendment A1:2013)
Published by DIN on July 1, 2013
This part of ISO 13408 specifies the requirements for isolator systems used for aseptic processing and offers guidance on qualification, bio-decontamination, validation, operation and control of...
This document is referenced by:
DIN EN ISO 13408-2 - Aseptic processing of health care products - Part 2: Sterilizing filtration (ISO 13408-2:2018)
Published by DIN on June 1, 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...
View Less
View All

Related Products

Searching for related products...

Advertisement