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Yjton Consulting - SFDA Medical Device registration China Clinical TrialsDESCRIPTION
Yjton Consulting - SFDA Medical Device registration China Clinical Trials. The China State Food and Drug Administration SFDA is the legal responsible unit of the Chinese government for medical device approval. All medical devices sold in China must be registered in SFDA before being introduced to the Chinese market. SFDA Medical Device Import Registration Certificates MDIRC must be renewed every four years. Find coordinators or assistance in your country through Jyton and Emergo worldwide offices.CONTENT
This web page jtmedical.blogspot.com states the following, "Yjton Consulting - SFDA Medical Device registration China Clinical Trials." We saw that the webpage said " The China State Food and Drug Administration SFDA is the legal responsible unit of the Chinese government for medical device approval." It also said " All medical devices sold in China must be registered in SFDA before being introduced to the Chinese market. SFDA Medical Device Import Registration Certificates MDIRC must be renewed every four years. Find coordinators or assistance in your country through Jyton and Emergo worldwide offices."