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ISO 14937

Sterilization of Health Care Products - General Requirements for Characterization of a Sterilizing Agent and the Development, Validation and Routine Control of a Sterilization Process for Medical Devices

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Organization: ISO
Publication Date: 15 December 2000
Status: inactive
Page Count: 45
ICS Code (Sterilization and disinfection in general): 11.080.01

Document History

ISO 14937
October 15, 2009
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
Inclusions This International Standard specifies general requirements for the characterization of a sterilizing agent and for the development, validation and routine monitoring and control of a...
ISO 14937
December 15, 2000
Sterilization of Health Care Products - General Requirements for Characterization of a Sterilizing Agent and the Development, Validation and Routine Control of a Sterilization Process for Medical Devices
A description is not available for this item.
14937
December 15, 2000
Sterilization of Health Care Products - General Requirements for Characterization of a Sterilizing Agent and the Development, Validation and Routine Control of a Sterilization Process for Medical Devices
A description is not available for this item.

References

This document is referenced by:
BS EN ISO 11737-1 + A1 - Sterilization of health care products - Microbiological methods Part 1: Determination of a population of microorganisms on products
Published by BSI on February 28, 2018
A description is not available for this item.
This document is referenced by:
BS EN ISO 13485 + A11 - Medical devices - Quality management systems - Requirements for regulatory purposes
Published by BSI on March 31, 2016
A description is not available for this item.
This document is referenced by:
BS EN ISO 17665-1 - Sterilization of health care products Moist heat Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by BSI on September 29, 2006
A description is not available for this item.
This document is referenced by:
BS EN 556-1 - Sterilization of Medical Devices - Requirements for Medical Devices to Be Designated "Sterile" - Part 1: Requirements for Terminally Sterilized Medical Devices
Published by BSI on December 11, 2001
A description is not available for this item.
This document is referenced by:
BS EN ISO 11138-1 - Sterilization of health care products — Biological indicators Part 1: General requirements
Published by BSI on April 30, 2017
A description is not available for this item.
This document is referenced by:
BS EN ISO 14630 - Non-active surgical implants - General requirements
Published by BSI on December 31, 2012
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.
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