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A China-US Joint Meeting Held For Medical Device Clinical Trial Supervision and Exchange


In this month, a Sino-US medical device clinical trial supervision exchange meeting was jointly held by the CFDA’s department of international cooperation, medical devices management department and the U.S. Food and Drug Administration (FDA) .

The conference invited the US FDA China Office experts,that the US clinical trials of medical devices regulations,FDA,sponsor,researchers and contract research organizations (CRO) responsibility, application and review of clinical trials of medical devices, as well as to the overseas medical device clinical data recognition etc. were introduced,Sino-American both sides also discussed the experiences and practices in the supervision of clinical trials of medical devices.


About China Med Device, LLC (CMD) CMD provides turn-key solution for Western medtech companies with regulatory and commercialization services. CMD helps its clients accelerate China entry and growth by offering: market Intelligence and research; CFDA regulatory services (premarket submission, clinical evaluation, clinical trial design & management, post market compliance and legal representation), and other commercial services. If you have an inquiry or feedback regarding our services please email us at

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