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2023-01-04
[R0001] Requirements for writing instructions for in vitro diagnostic reagents
2023-01-04
[R0002] Guidelines for Writing Technical Requirements for Medical Devices
2023-01-04
[R0003] Requirements for the first registration and application materials of in vitro diagnostic reagents
2023-01-04
[R0004] Risk management of medical devices
2023-01-04
[R0005] Requirements for application materials for continuing registration and changing registration of in vitro diagnostic reagents
2023-01-04
[R0006] EU in vitro diagnostic medical device regulation IVDR
2023-01-04
[R0007] New version of the Regulations on the Supervision and Administration of Medical Devices
2023-01-04
[R0008] Measures for the Supervision and Administration of Medical Device Operat
2023-01-04
[R0009] Unique identification of medical devices