DS/ISO 11607-2/AMD 1
Packaging for terminally sterilized medical devices – Part 2: Validation requirements for forming, sealing and assembly processes – Amendment 1: Application of risk management
active, Most Current
| Organization: | DS |
| Publication Date: | 20 September 2023 |
| Status: | active |
| Page Count: | 14 |
| 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 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.
Document History
DS/ISO 11607-2/AMD 1
September 20, 2023
Packaging for terminally sterilized medical devices – Part 2: Validation requirements for forming, sealing and assembly processes – Amendment 1: Application of risk management
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 20, 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...