CEN - EN ISO 11607-2
Packaging for terminally sterilized medical devices Part 2: Validation requirements for forming, sealing and assembly processes
active, Most Current
| Organization: | CEN |
| Publication Date: | 1 January 2020 |
| Status: | active |
| Page Count: | 42 |
| ICS Code (Sterilized packaging): | 11.080.30 |
scope:
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 does not cover all requirements for packaging medical devices that are manufactured aseptically. Additional requirements can be necessary for drug/device combinations.
Document History
EN ISO 11607-2
January 1, 2020
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 forming, sealing and...
January 1, 2020
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 forming, sealing and...
July 1, 2017
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
This part of ISO 11607 specifies the requirements for development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing,...
April 1, 2006
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
This part of ISO 11607 specifies the requirements for development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing,...
April 1, 2006
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
This part of ISO 11607 specifies the requirements for development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing,...