On March 24, 2026, NMPA published draft versions of registration review key points for 18 medical devices. Once finalized, the documents aim to provide manufacturers with clearer guidance on testing, clinical evaluation and registration requirements. This marks the second time that feedback has been sought for the key points concerning tumor gene variation detection reagents, […]
The post NMPA Review Key Points for Eighteen Devices Released in a Single Day, from Molecular Diagnostics to Additively Manufactured Orthopedics appeared first on China Med Device.




