DS/EN ISO 11137-3
Sterilization of health care products – Radiation – Part 3: Guidance on dosimetric aspects of development, validation and routine control (ISO 11137-3:2017)
active, Most Current
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| Organization: | DS |
| Publication Date: | 1 August 2017 |
| Status: | active |
| Page Count: | 54 |
| ICS Code (Sterilization and disinfection in general): | 11.080.01 |
scope:
ISO 11137-3:2017 gives guidance on meeting the requirements in ISO 11137-1 and ISO 11137-2 and in ISO/TS 13004 relating to dosimetry and its use in development, validation and routine control of a radiation sterilization process.
Document History
DS/EN ISO 11137-3
August 1, 2017
Sterilization of health care products – Radiation – Part 3: Guidance on dosimetric aspects of development, validation and routine control (ISO 11137-3:2017)
ISO 11137-3:2017 gives guidance on meeting the requirements in ISO 11137-1 and ISO 11137-2 and in ISO/TS 13004 relating to dosimetry and its use in development, validation and routine control of a...
August 14, 2006
Sterilization of health care products – Radiation – Part 3: Guidance on dosimetric aspects
This part of ISO 11137 gives guidance on the requirements in ISO 11137 parts 1 and 2 relating to dosimetry. Dosimetry procedures related to the development, validation and routine control of a...
Sterilization of health care products – Radiation – Part 3: Guidance on dosimetric aspects of development, validation and routine control (ISO/FDIS 11137-3:2016)
This part of ISO 11137 gives guidance on meeting the requirements in ISO 11137 parts 1 and 2 and in ISO TS 13004 relating to dosimetry and its use in development, validation and routine control of a...
Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects of development, validation and routine control (ISO/DIS 11137-3:2015)
This part of ISO 11137 gives guidance on meeting the requirements in ISO 11137 parts 1 and 2 and in ISO TS 13004 relating to dosimetry and its use in development, validation and routine control of a...