Registration number (WIID)Project No.TitleStatus
65418LVS EN ISO 11137-1:2015/A2:2020Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices - Amendment 2: Revision to 4.3.4 and 11.2 (ISO 11137-1:2006/Amd 2:2018)Standarts spēkā
67200FprEN ISO 18362Manufacture of cell-based health care products - Control of microbial risks during processing (ISO 18362:2016)Izstrādē
68124EN ISO 11737-1:2018/A1:2021Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms on products - Amendment 1 (ISO 11737-1:2018/Amd 1:2021)Standarts spēkā
68124LVS EN ISO 11737-1:2018/A1:2021Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms on products - Amendment 1 (ISO 11737-1:2018/Amd 1:2021)Standarts spēkā
68466EN ISO 13408-1:2024Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2023)Standarts spēkā
68466LVS EN ISO 13408-1:2024Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2023)Standarts spēkā
71095EN ISO 17665:2024Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665:2024)Standarts spēkā
71095LVS EN ISO 17665:2024Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665:2024)Standarts spēkā
72112EN ISO 25424:2019/A1:2022Sterilization of health care products - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices - Amendment 1 (ISO 25424:2018/Amd 1:2022)Standarts spēkā
72112LVS EN ISO 25424:2020/A1:2022Sterilization of health care products - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices - Amendment 1 (ISO 25424:2018/Amd 1:2022)Standarts spēkā
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