Medtech Advised To Prepare For Significant Updates In China’s Classification Catalogue

Revisions to China’s classification catalogue have now been finalized and they will have considerable impact on device registration, according to law firm Ropes & Gray.

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China's updated classification catalogue to come into effect in August 2018

Medtech companies operating in China are being advised to prepare for significant revisions the Chinese regulator has made to its 2002 Medical Device Classification Catalogue, which will become effective on Aug. 1, 2018.

The China Food and Drug Administration announced the final revision to the classification catalogue on Aug. 31, according to Katherine Wang, a partner at the Shanghai office of law firm...

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