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ClinicalClinical
+2+2
๐Ÿœ The China Clinical Trap
Feb 11, 2026

๐Ÿœ The China Clinical Trap

Common Mistakes of Manufacturers in Clinical Strategy

Elaine Tan
Medical DeviceMedical Device
+1+1
๐Ÿœ China Medtech: What You Missed in January
Jan 29, 2026

๐Ÿœ China Medtech: What You Missed in January

Catalogue updates, new guidance, standards watchlist

Elaine Tan
RegistrationRegistration
+2+2
๐Ÿœ China NMPA Revised Medical Device Classification Catalog
Jan 15, 2026

๐Ÿœ China NMPA Revised Medical Device Classification Catalog

What to do if your product is affected

Elaine Tan
Medical DeviceMedical Device
+1+1
๐Ÿœ China Regulatory 2025 Wrap Up
Dec 31, 2025

๐Ÿœ China Regulatory 2025 Wrap Up

What changed in 2025?

Elaine Tan
RegistrationRegistration
+2+2
๐Ÿœ Is Your EU Device Grouping Fit for China?
Dec 15, 2025

๐Ÿœ Is Your EU Device Grouping Fit for China?

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

Elaine Tan
ClinicalClinical
+2+2
๐Ÿœ Is Your EU MDR Clinical Evaluation Enough for China?
Nov 27, 2025

๐Ÿœ Is Your EU MDR Clinical Evaluation Enough for China?

Key differences between EU and China's CER

Elaine Tan
Medical DeviceMedical Device
+2+2
๐Ÿœ New China's GMP Update
Nov 13, 2025

๐Ÿœ New China's GMP Update

How China's GMP differs from ISO 13485?

Elaine Tan
RegistrationRegistration
+2+2
๐Ÿœ The Hidden Trap in Chinaโ€™s Type Testing
Oct 30, 2025

๐Ÿœ The Hidden Trap in Chinaโ€™s Type Testing

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

Elaine Tan
Medical DeviceMedical Device
+2+2
๐Ÿœ China's UDI Drafts in 2025
Oct 16, 2025

๐Ÿœ China's UDI Drafts in 2025

New Deadlines, Exemptions, and a Surprise Link to NHSA

Elaine Tan
Medical DeviceMedical Device
+1+1
๐Ÿœ Foreign Firms: Donโ€™t Miss Chinaโ€™s Self-Testing Shift
Oct 01, 2025

๐Ÿœ Foreign Firms: Donโ€™t Miss Chinaโ€™s Self-Testing Shift

Chinaโ€™s New Self-testing Guidance Explained

Elaine Tan
ClinicalClinical
+2+2
๐Ÿœ Success Stories of Real-World Data (Part 2)
Sep 18, 2025

๐Ÿœ Success Stories of Real-World Data (Part 2)

How Hainan became Chinaโ€™s medtech pilot zone

Elaine Tan
ClinicalClinical
+1+1
๐Ÿœ NMPA Approval with Real-World Data
Sep 05, 2025

๐Ÿœ NMPA Approval with Real-World Data

What If Your Clinical Data Isn't Enough?

Elaine Tan
Unlock Chinaโ€™s market access and regulatory compliance for medical devices.

Medtech Chopsticks

Unlock Chinaโ€™s market access and regulatory compliance for medical devices.

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