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Norm
ISO 11607-2:2019
Issue date: 2019 01 31
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes
This document specifies requirements for the development and validation of processes for packaging medical devices that are terminally sterilized. These processes include...
Valid
Publisher:
International Organization for Standardization
Format:
Digital | 13 Pages
Language:
English
ICS
This document specifies requirements for the development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing and assembly of preformed sterile barrier systems, sterile barrier systems and packaging systems.
It is applicable to industry, to health care facilities, and to wherever medical devices are packaged and sterilized.
It does not cover all requirements for packaging medical devices that are manufactured aseptically. Additional requirements can be necessary for drug/device combinations.
ISO 11607-2:2019
2019 01 31
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, s...
Norm
↖
ISO 11607-2:2006/Amd 1:2014
2014 07 07
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, s...
Norm
ISO 11607-2:2006
2006 04 07
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, s...
Norm
Norm
Issue date :
2023 09 13
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes — Amendment 1: Application of risk management
