医疗器械监督管理系统条例第650令英文翻译版本Word下载.docx
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医疗器械监督管理系统条例第650令英文翻译版本Word下载.docx
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TheRegulationsfortheSupervisionandManagementofMedicalDevices,revisedatthe39thexecutivemeetingoftheStataCouncilonFebruary12,2014,isherebypromulgatedandshallgointoeffectasofJune1,2014.
Premier:
LiKeqiang
March7,2014
(PromulgatedastheDecreeoftheStateCouncilofthePeople’sRepublicofChinaNo.276onJanuary4,2000,andrevisedatthe39thexecutivemeetingoftheStataCouncilonFebruary12,2014.)
ChapterIGeneralProvisions
Article1TheRegulationsareherebyformulatedwithaviewtoguaranteeingthesafetyandeffectivenessofmedicaldevicesandprotectinghumanhealthandlifesafety.
Article2Allunitsorindividualsengagedintheresearchanddevelopment,production,distribution,use,supervisionandmanagementofmedicaldeviceswithintheterritoryofthePeople'
sRepublicofChinashallcomplywiththeRegulation.
Article3ThefoodanddrugsupervisionandmanagementdepartmentoftheStateCouncilshallberesponsibleforthesupervisionandmanagementofnationalmedicaldevices.RelevantdepartmentsoftheStateCouncilshallberesponsibleforthesupervisionandmanagementrelatingtomedicaldeviceswithinrespectivetermofreference.
Thefoodanddrugsupervisionandmanagementdepartmentofthelocalpeople’sgovernmentabovethelevelofcountyshallberesponsibleforthesupervisionandmanagementofmedicaldeviceswithinrespectiveadministrativeregion.Relevantdepartmentsofthelocalpeople’sgovernmentsabovethelevelofcountyshallberesponsibleforthesupervisionandmanagementrelatingtomedicaldeviceswithinrespectivetermofreference.
ThefoodanddrugsupervisionandmanagementdepartmentoftheStateCouncilshallsupporttherelevantdepartmentsoftheStateCouncilintheimplementationofthenationalindustrialplansandpoliciesonmedicaldevices.
Article4TheStateshallimplementclassifiedmanagementonmedicaldevicesbasedonthedegreeofrisk.
ClassIMedicalDevicesarethosewithlowerdegreeofriskforwhichthesafetyandeffectivenesscanbeensuredthroughroutinemanagement;
ClassIIMedicalDevicesarethosewithmediumdegreeofriskforwhichfurthercontrolisrequiredtoensuretheirsafetyandeffectiveness
ClassIIIMedicalDevicesarethosewithhigherdegreeofriskwhichmustbestrictlycontrolledinrespecttosafetyandeffectiveness.
Evaluationondegreeofriskshouldtakeintoaccounttheanticipatedpurpose,structuralcharacteristics,usage,andotherfactorsofmedicaldevices.
ThefoodanddrugsupervisionandmanagementdepartmentoftheStateCouncilshallberesponsibleforformulatingtheclassificationrulesandclassifiedcatalogofmedicaldevices,conducttimelyanalysisandevaluationonthechangeofproductriskaccordingtotheproduction,distribution,anduseofthemedicaldevices,andadjustclassifiedcatalog.Whenformulatingandadjustingtheclassifiedcatalog,thefoodanddrugsupervisionandmanagementdepartmentoftheStateCouncilshallfullylistentotheopinionsofthemedicaldevicemanufacturingandoperatingenterprises,usingunits,andindustrialorganizations,andconsultinginternationalclassificationpracticesofmedicaldevices.Theclassifiedcatalogshouldbemadepublic.
Article5TheR&
Dofmedicaldevicesshallbebasedontheprincipleofsafety,effectivenessandpracticingeconomy.TheStatewhilegivingplaytotheroleofmarketmechanismencouragestheresearchanddevelopmentandinnovationofmedicaldevices,booststheapplicationandgeneralizationofnewtechnologyofmedicaldevices,andpromotesthedevelopmentofmedicaldeviceindustry.
Article6Medicaldeviceproductsshallcomplywiththecompulsorynationalstandardformedicaldevices;
ifthecompulsorynationalstandardisunavailable;
complywiththecompulsoryindustrialstandardformedicaldevices.
Thecatalogofdisposablemedicaldevicesshallbeformulated,adjustedandpublishedbythefoodanddrugsupervisionandmanagementdepartmentoftheStateCounciltogetherwiththecompetenthealthandfamilyplanningdepartmentoftheStateCouncil.Medicaldevicesthatcanguaranteeitssafetyandeffectivenesswhenreusedshallnotbeincludedinthecatalog.Formedicaldevicesthatcanguaranteeitssafetyandeffectivenesswhenreusedafterimprovementsinitsdesign,productionprocessandsterilizationtechnology,etc.,theyshallberuledoutfromthecatalog.
Article7Themedicaldevicesindustrialorganizationshouldstrengthenindustrialself-discipline,promotecreditsystemconstruction,urgeenterprisestoconductproductionandoperationactivitiesaccordingtolaw,andguideenterprisestobehonestandtrustworthy.
ChapterIIRegistrationandFilingofMedicalDeviceProducts
Article8ProductfilingmanagementshallbeimplementedonClassImedicaldevices.ProductregistrationmanagementshallbeimplementedonClassIIandClassIIImedicaldevices.
Article9ThefollowingmaterialsshouldbesubmittedforthefilingofClassImedicaldeviceproductsandapplicationfortheregistrationofClassIIandClassIIImedicaldeviceproducts.
(I)Productriskanalysismaterials;
(II)Producttechnicalrequirements;
(III)Productinspectionreport;
(IV)Clinicalevaluationmaterials;
(V)Productinstructionandlabelsample;
(VI)Qualitymanagementsystemdocumentsrelatedtoproductresearch&
manufactureandproduction;
(VII)Othermaterialsnecessaryfordemonstratingthesafetyandeffectivenessofthemedicaldevice.
Theregistrationapplicantandfilingapplicantofmedicaldevicesshallberesponsiblefortheauthenticityofthematerialssubmitted.
Article10ForthefilingofClassImedicaldeviceproduct,thefilingapplicantshallsubmitfilingmaterialstothefoodanddrugsupervisionandmanagementdepartmentofthepeople’sgovernmentofthemunicipalityestablishedwithdistricts;
inwhich,productinspectionreportmaybetheself-inspectionreportofthefilingapplicant;
clinicalevaluationmaterialsexcludeclinicaltrialreportbutmaybethematerialsdemonstratingthesafetyandeffectivenessthroughreferencesandthedataobtainedfromtheclinicalapplicationofsimilarproducts.
TheoverseasmanufacturingenterpriseexportingClassImedicaldevicetotheterritoryofthePeople’sRepublicofChinashall,throughitsrepresentativeofficeestablishedwithintheterritoryofthePeople’sRepublicofChinaorthebusinessentitydesignatedwithintheterritoryofthePeople’sRepublicofChinaastheagent,submitfilingmaterialsandtheevidentialdocumentsapprovedbythecompetentdepartmentofthecounty(region)wherethefilingapplicantislocatedformarketingofthemedicaldevicetothefoodanddrugsupervisionandmanagementdepartmentoftheStateCouncil.
Incaseofanychangetothemattersspecifiedinthefilingmaterials,filingapplicantshouldapplyforthefilingofchangewiththeoriginalfilingdepartment.
Article11FortheapplicationfortheregistrationofClassIImedicaldeviceproducts,registrationapplicantshouldsubmitregistrationmaterialstothefoodanddrugsupervisionandmanagementdepartmentofthepeople’sgovernmentoftheprovince,autonomousregion,ormunicipalitydirectlyunderthecentralgovernmentwheretheapplicantislocated.FortheapplicationforregistrationofClassIIImedicaldeviceproducts,registrationapplicantshouldsubmitregistrationmaterialstothefoodanddrugsupervisionandmanagementdepartmentoftheStateCouncil.
OverseasmanufacturingenterpriseexportingClassIIandClassIIImedicaldevicestotheterritoryofthePeople’sRepublicofChina,shouldthroughitsrepresentativeofficeestablishedwithintheterritoryofthePeople’sRepublicofChinaorthebusinessentitydesignatedwithintheterritoryofthePeople’sRepublicofChinaasitsagent,submitregistrationmaterialsandtheevidentialdocumentsapprovedbythecompetentdepartmentofthecounty(region)wheretheregistrationapplicantislocatedformarketingofthemedicaldevicetothefoodanddrugsupervisionandmanagementdepartmentoftheStateCouncil.
TheproductinspectionreportintheregistrationmaterialsofClassIandClassIImedicaldeviceproductsshouldbetheinspectionreportissuedbymedicaldeviceinspectionagency;
clinicalevaluationmaterialsshouldincludeclinicaltrialreport,exceptforthemedicaldevicesexemptedfromclinicaltrialaccordingtotheArticle17inthisRegulation.
Article12Thefoodanddrugsupervisionandmanagementdepartmentacceptingregistrationapplicationshallputforwardtheapplicationmaterialstotechnicalevaluationinstitutionwithin3workingdaysafterthedateofacceptance.Technicalevaluationinstitutionshouldcompletethetechnicalevaluationandthensubmitevaluationopiniontothefoodanddrugsupervisionandmanagementdepartment.
Article13Thefoodanddrugsupervisionandmanagementdepartmentacceptingregistrationapplicationshouldmakedecisionwithin20workingdaysafterreceivingtheevaluationopinion.Forthosecomplyingwiththerequirementsonsafetyandeffectiveness,registrationisapprovedandtheMedicalDeviceRegistrationCertificateshallbeissued;
forthosenotcomplyingwiththerequirements,theregistrationshallnotbeapprovedandthereasonsshallbespecifiedinwritten.
WhenthefoodanddrugsupervisionandmanagementdepartmentoftheStateCouncilorganizesthetechnicalevaluationonimportedmedicaldevices,ifitdeemsnecessarytoinspectthequalitymanagementsystem,thefood
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