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BSI - BS EN ISO 14644-7

Cleanrooms and associated controlled environments - Part 7: Separative devices (clean air hoods, gloveboxes, isolators and mini-environments)

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Organization: BSI
Publication Date: 14 October 2004
Status: active
Page Count: 64
ICS Code (Cleanrooms and associated controlled environments): 13.040.35

Document History

BS EN ISO 14644-7
October 14, 2004
Cleanrooms and associated controlled environments - Part 7: Separative devices (clean air hoods, gloveboxes, isolators and mini-environments)
A description is not available for this item.

References

This document references:
BS EN ISO 13408-1 - Aseptic processing of health care products Part 1: General requirements
Published by BSI on August 31, 2015
A description is not available for this item.
This document references:
ISO 10648-1 - Containment Enclosures - Part 1: Design Principles
Published by ISO on May 15, 1997
A description is not available for this item.
This document references:
ISO 10648-2 - Containment Enclosures - Part 2: Classification According to Leak Tightness and Associated Checking Methods
Published by ISO on December 15, 1994
A description is not available for this item.
This document references:
ENV 1631 - Cleanroom Technology - Design, Construction and Operation of Cleanrooms and Clean Air Devices
Published by CEN on July 1, 1996
A description is not available for this item.
This document references:
BS EN ISO 13408-1 - Aseptic processing of health care products Part 1: General requirements
Published by BSI on August 31, 2015
A description is not available for this item.
This document references:
BS EN ISO 13408-5 - Aseptic processing of health care products Part 5: Sterilization in place
Published by BSI on October 30, 2011
A description is not available for this item.
This document references:
BS EN ISO 13408-1 - Aseptic processing of health care products Part 1: General requirements
Published by BSI on August 31, 2015
A description is not available for this item.
This document references:
BS EN ISO 13408-5 - Aseptic processing of health care products Part 5: Sterilization in place
Published by BSI on October 30, 2011
A description is not available for this item.
This document is referenced by:
BS EN ISO 15378 - Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2008, with reference to Good Manufacturing Practice (GMP)
Published by BSI on November 30, 2015
A description is not available for this item.
This document is referenced by:
BS EN ISO 11737-2 - Sterilization of health care products - Microbiological methods Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process
Published by BSI on May 31, 2020
A description is not available for this item.
This document is referenced by:
BS EN ISO 29701 - Nanotechnologies - Endotoxin test on nanomaterial samples for in vitro systems - Limulus amebocyte lysate (LAL) test
Published by BSI on October 31, 2010
A description is not available for this item.
This document is referenced by:
BS ISO 15388 - Space systems - Contamination and cleanliness control
Published by BSI on February 29, 2012
A description is not available for this item.
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