CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 78646 | prEN ISO 14937 | 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 | Izstrādē |
| 9291 | - | Method(s) of bioburden determination - Methods for validating bioburden techniques | Izstrādē |
| 76997 | CEN ISO/TS 11137-4:2023 | Sterilization of health care products - Radiation - Part 4: Guidance on process control (ISO/TS 11137-4:2020) | Izstrādē |
| 62287 | prEN ISO 17665-1 rev | Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices | Izstrādē |
| 9288 | prEN 555 | Sterilization of medical devices - Method for validation and routine control of steam sterilization - Guidance | Izstrādē |
| 31155 | prEN ISO 11137-2 | Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose | Izstrādē |
| 9310 | prEN ISO 11137-3 | Sterilization of medical devices - Microbiological methods - Part 3: Guidance on the evaluation and interpretation of bioburden data | Izstrādē |
| 78154 | FprCEN ISO/TS 17664-3 | Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 3: Guidance on the designation of a reusable medical device to a cleaning classification (ISO/DTS 17664-3:2026) | 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 11-20 of 179 results.