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.
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