CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 39976 | EN ISO 11137-3:2017 | Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects of development, validation and routine control (ISO 11137-3:2017) | Izstrādē |
| 79283 | prEN ISO 11737-1 rev | Sterilization of health care products — Microbiological methods — Part 1: Determination of a population of microorganisms on products | Izstrādē |
| 21959 | CEN/TC 204 N 470 | Sterilization of medical devices - Development, validation and routine control of sterilization processes - Low Temperature Steam and Formaldehyde | Izstrādē |
| 82878 | prEN ISO 11737-3 | Sterilization of health care products - Microbiological methods - Part 3: Bacterial endotoxin testing (ISO 11737-3:2023) | Izstrādē |
| 80418 | prEN ISO 11137-2 rev | Sterilization of health care products — Radiation — Part 2: Establishing the sterilization dose | Izstrādē |
| 82923 | EN ISO 14937:2009/prA1 | Sterilization of health care products — General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices — Amendment 1 | Izstrādē |
| 82958 | EN ISO 17665:2024/prA1 | Sterilization of health care products — Moist heat — Requirements for the development, validation and routine control of a sterilization process for medical devices — Amendment 1 | Izstrādē |
| 9291 | - | Method(s) of bioburden determination - Methods for validating bioburden techniques | Izstrādē |
| 67200 | FprEN ISO 18362 | Manufacture of cell-based health care products - Control of microbial risks during processing (ISO 18362:2016) | Izstrādē |
| 80410 | EN ISO 13408-1:2024/prA1 | Aseptic processing of health care products — Part 1: General requirements — Amendment 1 | Izstrādē |
Displaying 1-10 of 176 results.