CEN/TC 206
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 40814 | prEN ISO 10993-5 rev | Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009) | Izstrādē |
| 40661 | prEN ISO 10993-7 rev | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals | Izstrādē |
| 84211 | prEN ISO 14155 rev | Clinical investigation of medical devices for human subjects — Good clinical practice | Izstrādē |
| 77335 | prEN ISO 18969 | Clinical evaluation of medical devices (ISO/DIS 18969:2025) | Izstrādē |
| 78812 | prEN ISO 21762 | Medical devices utilizing non-viable human materials - Risk management (ISO/DIS 21762:2025) | Izstrādē |
| 84561 | prEN ISO 22442-1 rev | Medical devices utilizing tissues and their derivatives — Part 1: Application of risk management | Izstrādē |
| 84560 | prEN ISO 22442-2 rev | Medical devices utilizing tissues and their derivatives — Part 2: Controls on sourcing, collection and handling | Izstrādē |
| 80886 | prEN ISO 22442-3 rev | Medical devices utilizing animal tissues and their derivatives — Part 3: Validation of the elimination and/or inactivation of viruses and transmissible spongiform encephalopathy (TSE) agents | Izstrādē |
| 81042 | prEN ISO 8250 | Cleanliness of medical devices - Process design and test methods | Izstrādē |
| 76054 | prEN ISO 8250 | Cleanliness of medical devices -- Process design and test methods | Izstrādē |
Displaying 191-200 of 200 results.