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CFDA to Start Priority Reviews of Medical Devices in January 2017

publication date: Nov 2, 2016
Starting in January 2017, the CFDA will begin accepting priority review applications for medical devices, a parallel effort to the priority reviews established for new drugs. To qualify, the medical device must offer a significant advance in terms of clinical practice or be derived from a National Science and Technology Major Project or National Key Research and Development Plan. The priority pathway is open to Class III domestically manufactured devices and Class II or III imported devices. More details....

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