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ISO 13408-5

Aseptic processing of health care products Part 5: Sterilization in place

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Organization: ISO
Publication Date: 15 November 2006
Status: active
Page Count: 22
ICS Code (Sterilization and disinfection in general): 11.080.01

Document History

ISO 13408-5
November 15, 2006
Aseptic processing of health care products Part 5: Sterilization in place
A description is not available for this item.

References

This document is referenced by:
SN EN ISO 14160 - Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices
Published by SNV on August 1, 2021
This document specifies requirements for the characterization of a liquid chemical sterilizing agent and for the development, validation, process control and monitoring of sterilization by liquid...
This document is referenced by:
ISO 13022 - Medical products containing viable human cells - Application of risk management and requirements for processing practices
Published by ISO on April 1, 2012
This International Standard specifies requirements and guidance for processing practices and managing risk associated with viable cellular components of products regulated as medicinal products,...
This document is referenced by:
BS EN ISO 14160 - Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices
Published by BSI on July 31, 2011
A description is not available for this item.
This document is referenced by:
AAMI 14160 - Sterilization of health care products — Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives — Requirements for characterization, development, validation and routine control of a sterilization process for medical devices
Published by AAMI on January 1, 2011
This International Standard specifies requirements for the characterization of a liquid chemical sterilizing agent and for the development, validation, process control and monitoring of sterilization...
This document is referenced by:
ISO 13408-3 - Aseptic processing of health care products Part 3: Lyophilization
Published by ISO on September 15, 2006
This part of ISO 13408 specifies requirements for, and offers guidance on, equipment, processes, programmes and procedures for the control and validation of lyophilization as an aseptic process. It...
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