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 14644-3

Cleanrooms and associated controlled environments - Part 3: Test methods (ISO 14644-3:2005)

inactive
Buy Now
Organization: DIN
Publication Date: 1 March 2006
Status: inactive
Page Count: 71
ICS Code (Cleanrooms and associated controlled environments): 13.040.35

Document History

DIN EN ISO 14644-3
August 1, 2020
Cleanrooms and associated controlled environments - Part 3: Test methods (ISO 14644-3:2019, Corrected version 2020-06)
A description is not available for this item.
DIN EN ISO 14644-3
February 1, 2017
Cleanrooms and associated controlled environments - Part 3: Test methods (ISO/DIS 14644-3:2016); German and English version prEN ISO 14644-3:2016
A description is not available for this item.
DIN EN ISO 14644-3
March 1, 2006
Cleanrooms and associated controlled environments - Part 3: Test methods (ISO 14644-3:2005)
A description is not available for this item.

References

This document is referenced by:
DIN EN ISO 15378 - Primaerpackmittel fuer Arzneimittel - Besondere Anforderungen fuer die Anwendung von ISO 9001:2015 entsprechend der Guten Herstellungspraxis (GMP) (ISO 15378:2017); Deutsche Fassung EN ISO 15378:2017
Published by DIN on April 1, 2018
Diese Internationale Norm legt Anforderungen an ein Qualitätsmanagementsystem fest, wenn eine Organisation a) ihre Fähigkeit darlegen muss, beständig Produkte und Dienstleistungen bereitstellen zu...
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 15378 - Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) (ISO 15378:2017)
Published by DIN on April 1, 2018
This International Standard specifies requirements for a quality management system when an organization: a) needs to demonstrate its ability to consistently provide products and services that meet...
This document is referenced by:
DIN EN ISO 15883-1 - Washer-disinfectors - Part 1: General requirements, terms and definitions and tests (ISO 15883-1:2006 + Amd 1:2014) (includes Amendment A1:2014)
Published by DIN on October 1, 2014
This part of ISO 15883 specifies general performance requirements for washer-disinfectors (WD) and their accessories that are intended to be used for cleaning and disinfection of re-usable medical...
View Less
View All
Advertisement