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RegistrationPost-marketClinicalMedical DeviceTestingInnovativeChina AgentChina
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🍜 Potential Changes to China's Medical Device Classification Rules
May 29, 2025

🍜 Potential Changes to China's Medical Device Classification Rules

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

Elaine Tan
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🍜 Secure Made‐in‐China Approval by Moving Production to China
Apr 21, 2025

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

Elaine Tan
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🍜 Navigating the NMPA Registration Process: Timelines, Costs, and Considerations
Mar 18, 2025

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

Elaine Tan
Dive into market access and regulatory compliance of medical devices in China

Medtech Chopsticks

Dive into market access and regulatory compliance of medical devices in China

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