CEN/CLC/TC 3
| Project No. | - |
|---|---|
| Title | This Technical Report provides guidance on the relationship between CEN ISO TR 20416:2020 (Medical devices – Post-market surveillance for manufacturers) and the requirements in the European Regulations on Medical Devices (MDR)- Regulation (EU) 2017/745 - and In Vitro Diagnostic Medical Devices (IVDR) -Regulation (EU) 2017/746. |
| Registration number (WIID) | 72189 |
| Scope | This Technical Report provides guidance on the relationship between CEN ISO TR 20416:2020 (Medical devices – Post-market surveillance for manufacturers) and the requirements in the European Regulations on Medical Devices (MDR)- Regulation (EU) 2017/745 - and In Vitro Diagnostic Medical Devices (IVDR) -Regulation (EU) 2017/746. |
| Status | Izstrādē |
| ICS group | Not set |