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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China Commercialization Turn-Key Solutions

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China Commercialization Turn-Key Solutions
Market AssessmentNMPA (CFDA) RegistrationCER & Clinical TrialGMP/Post MarketKOL & White PaperMarketing PromotionDistribution ManagementTechnology LicensingStrategic Funding

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...

CER & Clinical Trial

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GMP/Post Market

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KOL & White Paper

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Marketing Promotion

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Distribution Management

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Technology Licensing

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Strategic Funding

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THE CHINA COMMERCIALIZATION PROCESS

We Have Helped 50+ U.S Medtech Companies
Enter China's Medical Marketplace