ISO/TC 198
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 86251 | ISO/PWI 13408-4 | Aseptic processing of health care products — Part 4: Clean-in-place technologies | Izstrādē |
| 53727 | ISO/NP 13408-8 | Aseptic processing of health care products — Part 8: Cell-based health care products | Izstrādē |
| 91839 | ISO/AWI TS 25887 | Sterilization of health care products — Microbiological methods — Bacterial endotoxin testing — Use of recombinant animal-free reagents | Izstrādē |
| 93090 | ISO 14937:2009/WD Amd 1 | 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 |
| 36113 | ISO/TR 13409:1996/CD Amd 1 | Sterilization of health care products — Radiation sterilization — Substantiation of 25 kGy as a sterilization dose for small or infrequent production batches — Amendment 1 | Izstrādē |
| 39384 | ISO/NP 16342 | Sterilization of health care products — Method for validation of a biological indicator incubation period | Izstrādē |
| 54072 | ISO/NP 11140-6 | Sterilization of health care products — Chemical indicators — Part 6: Class 2 indicators and process challenge devices for use in performance testing of steam sterilizers | Izstrādē |
| 30063 | ISO/CD 13408-6 | Aseptic processing of health care products — Part 6: Isolator/barrier technology | Izstrādē |
| 35049 | ISO/WD 11140-5 | Sterilization of health care products — Chemical indicators — Part 5: Class 2 indicators for air removal test sheets and packs | Izstrādē |
| 33954 | ISO/WD 11137-3 | Sterilization of health care products — Requirements for the development, validation and routine control of a sterilization process for medical devices — Radiation — Part 3: Dose substantiation of 25-kGy method | Izstrādē |
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