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China Food and Drug Administration Issues Technical Review Guidelines for the Registration of Medical Device Software

date：2015-08-25 15:52:54
On August 5, 2015, the China Food and Drug Administration (CFDA) issued the Technical Review Guidelines for the Registration of Medical Device Software. These guidelines are intended to guide manufacturers in submitting registration application materials for medical device software and standardize the technical review requirements for such software.
For details, please click the link to view: http://www.sfda.gov.cn/WS01/CL1103/126260.html


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