dimarts, 12 d’agost del 2014

Further analysis of new Chinese medical device registration requirements




The Emergo Group Blog provides short updates on quality and regulatory topics that may be of interest to QA/RA professionals in the medical device and IVD industry. No fluff, just straight to the point. We hope you'll enjoy the content.





Further analysis of new Chinese medical device registration requirements

By Stewart Eisenhart, Emergo Group


Emergo Group colleagues in China have provided additional details on recently published changes to the China Food and Drug Administration's (CFDA) medical device registration process.




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