Registration

🍜 Is Your EU Device Grouping Fit for China?

Key differences between EU Basic UDI-DI and China Registration Unit

🍜 The Hidden Trap in China’s Type Testing

Why your ISO/IEC compliance might still fail NMPA tests.

🍜 Potential Changes to China's Medical Device Classification Rules

New draft rules sharpen the line between Class I and Class II devices

🍜 Secure Made‐in‐China Approval by Moving Production to China

🍜 Navigating the NMPA Registration Process: Timelines, Costs, and Considerations