AccordingtotheCOVID-19preventionandcontrolneeds,inordertoensurethetreatmentofsevereCOVID-19patients,theNationalMedicalProductsAdministrationofChina(NMPA)urgentlyapprovedtheregistrationapplicationsofth...
Toallinstitutionsconcerned,TheNationalMedicalProductsAdministrationofChina(NMPA)issuedtheAnnouncementontheRegistrationMattersofMedicalDeviceMasterFiles(No.36of2021)inMarch2021,andtheCenterforMedicalDe...
WiththereleaseofAnnouncementNo.40oftheCenterforMedicalDeviceEvaluation,NMPA(hereinafterreferredtoasthe“CMDE”),GuidingPrinciplesforReviewofRegistrationofClinicalEvaluationsofGeneSequencers,onNovember...
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