China Medical Device - Accelerate Your Medical Device's Entry Into China

WHY CMD?
REGULATORY SERVICES
BUSINESS SERVICES

BI-LINGUAL &
BI-CULTURAL EXPERTISE

20 years seasoned proven bi-lingual and bi-cultural staff with medtech domain knowledge

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NMPA (CFDA) PREMARKET
SUBMISSIONS

Unique and integrated approach for NMPA (CFDA) premarket submission: Technical+Clinical+Regulatory

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RESOURCES ARE
KEY

Resources to clinical societies, key opinion leaders, decision makers in medical device/IVD companies and large distribution network

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NEW WEBINAR!

Latest Developments in Clinical Pathways
for NMPA (CFDA) Submission

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China Commercialization Turn-Key Solutions

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Market Assessment

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NMPA (CFDA) Registration

China medical device/In-Vitro Diagnostic (IVD) regulations are ever-changing with increasing complexity. It’s essential to have an integrated and experienced team help your organization develop the customized registration strategy needed to gain NMPA (CFDA) approval for any medical device/IVD to be marketed and sold in China. Read More...