Department of Commerce and China's State Food and Drug Administration (SFDA) have agreed to harmonize standards for medical devices being developed, so that China can become a more successful player in the medtech sector. In the talks, the two parties discussed ways to further streamline ChinaâEUR(TM)s device registration process. ChinaâEUR(TM)s SFDA delegates explained their countryâEUR(TM)s new adverse event reporting regulation.
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