英文版医疗器械临床试验质量管理规范.docx
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英文版医疗器械临床试验质量管理规范.docx
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英文版医疗器械临床试验质量管理规范
FG-20160601025
GoodClinicalPracticeforMedicalDevices
(No.25OrderofCFDAandNHFPC)
OrderofChinaFoodandDrugAdministrationandNationalHealthandFamilyPlanningCommissionofChina
No.25
AdoptedatthemeetingofCFDAandNHFPC,thispracticeisherebypromulgated,andshalltakeeffectasofJune1,2016.
Director BiJingquan
DirectorLiBin
March1,2016
GoodClinicalPracticeforMedicalDevices
Chapter1Generalprovisions
Article1ThePracticeisformulatedinaccordancewiththeRegulationsontheSupervisionandAdministrationofMedicalDevicesinordertofurtherstrengthenthemanagementofclinicaltrialsofmedicaldevices,protecttherightsandbenefitsoftrialsubjectsandassuretheclinicaltrialprocedurestandard,truthful,scientific,reliableandtraceable.
Article2AlltheclinicaltrialsofmedicaldeviceswithintheterritoryofthePeople'sRepublicofChinashallbeconductedaccordingtothepractice.ThePracticecoversthewholeprocedureofclinicaltrialofmedicaldevices,includingtheprotocoldesign,conduction,monitoring,audit,inspection,collectionofdata,record,analysisandsummaryandreportofclinicaltrial,etc.
Article3ClinicaltrialofmedicaldevicesmentionedinthisPracticereferstotheprocessofconfirmingandverifyingthesafetyandefficacyofthemedicaldeviceintendedtoapplyregistrationundernormalconditioninqualifiedclinicaltrialinstitutionsofmedicaldevices.
Article4Clinicaltrialsofmedicaldevicesshallcomplywiththeprincipleoflegal,ethicandscience.
Article5Foodanddrugregulatoryauthorityaboveprovincelevelareresponsibleforthesupervisionandmanagementofclinicaltrailsofmedicaldevices.
ThecompetentdepartmentofNationalHealthandFamilyPlanningCommissionshallstrengthenthemanagementofclinicaltrailsofmedicaldeviceswithin the scope of its duties.
FoodanddrugregulatoryauthorityandthecompetentdepartmentofNHFPCshallestablishtheinformationnotificationsystemonqualitymanagementofmedicaldeviceclinicaltrialsandstrengthentheinformationnotificationontheapprovalforconductingclinicaltrialofClassIIImedicaldevicesandthemedicaldeviceslistedinthemanagementcatalogoflarge medical equipmentcollocation in Chinaandthedataofthesupervisionandmanagementonrelevantclinicaltrial.
ChapterIIPreparationbeforeclinicaltrials
Article6Thereshouldbesufficientscientificbasisandcleartrialpurposetoconductclinicaltrialsofmedicaldevices,andtheexpectedbenefitsandriskstothehealthofsubjectsandpublicshallbeweighed,theexpectedbenefitsshouldexceedthepossibledamage.
Article7Beforeclinicaltrial,thesponsorshallcompletethepre-clinicalstudyofinvestigationalmedicaldevices,includingthedesignofproducts(structureandcomposition,workingprincipleandmechanismofaction,intendeduse,applicationscopeandapplicabletechnicalrequirements)andqualityinspection,animaltrialandanalysisreport,etc,andtheresultsshallsupporttheclinicaltrial.Theresultsofqualityinspectionincludereportofself-inspectionandthequalifiedreportforregistrationinspectionissuedbyaqualifiedinspectionagencywithinoneyear.
Article8Beforeclinicaltrial,thesponsorshallprepareadequateinvestigationalmedicaldevices.Thedevelopmentofinvestigationalmedicaldevicesshallmeetrelevantrequirementsofqualitymanagementsystemofmedicaldevices.
Article9Clinicaltrialsofmedicaldevicesshallbeconductedintwoormorethantwoclinicaltrialinstitutionsofmedicaldevices.Theselectedtrailinstitutionshallbequalifiedclinicaltrialinstitutionofmedicaldevicesandthefacilitiesandconditionsshallmeettherequirementsforconductingclinicaltrialssafelyandeffectively.Theinvestigatorshouldhavetheprofessionalexpertise,qualificationsandabilitytoundertaketheclinicaltrialandshouldhavebeentrained.
Administrativemeasuresforthequalification recognitionofclinicaltrialinstitutionsofmedicaldevices shall be formulated separately byChinaFoodandDrugAdministrationandNationalHealthandFamilyPlanningCommissionofChina.
Article10Beforeclinicaltrial,thesponsor,clinicaltrialinstitutionandinvestigatorshallmakea written agreementontrialdesign,qualitycontroloftrial,divisionofresponsibilitiesinthetrial,thecostofclinicaltrialsundertakenbythesponsorandthetreatmentprincipleofinjuriesthatmayoccurinthetrial.
Article11Clinicaltrialsshouldbeapprovedbyethicscommitteeofclinicaltrialinstitutions.MedicaldeviceslistedinthedirectoryofClassIIImedicaldeviceclinicaltrialshallalsobeapprovedbyCFDA.
Article12Beforeclinicaltrial,thesponsorshouldfiletolocalfoodanddrugregulatoryauthorityoftheprovince,theautonomousregionorthemunicipalitydirectlyundertheCentralGovernment.
ThefoodanddrugregulatoryauthorityacceptingthefillingshouldreportthefilingsituationstothefoodanddrugregulatoryauthorityandthecompetentauthorityofNHFPCinthesamelevelwheretheclinicaltrialinstitutionislocated.
ChapterIIIProtectionofrightsandbenefitsoftrialsubjects
Article13ClinicaltrialsofmedicaldevicesshouldbeconductedinaccordancewiththeethicalprinciplesinWorldMedicalAssociationDeclarationofHelsinki.
Article14Ethicalreviewandinformedconsentarethemainmeasurestoprotecttherightsandbenefitsofsubjects.Eachpartyinvolvedintheclinicaltrialshallundertakecorrespondingethicalresponsibilitiesaccordingtotheirdutiesinthetrial.
Article15Thesponsorshouldavoidtocauseundueinfluenceormisleadingtosubjects,clinicaltrialinstitutionsandtheinvestigatorandotherclinicaltrialparticipantsorrelatedparties.
Clinicaltrialinstitutionandtheinvestigatorshouldavoidtocauseundueinfluenceandmisleadingtosubjects,thesponsorandotherclinicaltrialparticipantsorrelatedparties.
Article16Thesponsor,clinicaltrialinstitutionandtheinvestigatorshallnotexaggeratethecompensationmeasuresforparticipatinginclinicaltrialsandmisleadthesubjectstoparticipateinclinicaltrials.
Article17Beforeclinicaltrial,thesponsorshallsubmitthefollowingdocumentstoethicscommitteethroughtheinvestigatorandthemanagementdepartmentofmedicaldeviceclinicaltrialofclinicaltrialinstitution:
(1)Protocolofclinicaltrial;
(2)Investigator’sbrochure;
(3)Textofinformedconsentformandanyotherwrittendocumentsprovidedtosubjects;
(4)Procedural documentsforrecruitingsubjectsandpublicity;
(5)Textofcasereportform;
(6)Self-inspectionreportandtheinspectionreportforproductregistration;
(7)Resumes,professionalexpertise,ability,trainingoftheinvestigatorandotherdocumentstoprovequalifications;
(8)Overviewofthefacilitiesandconditionsofclinicaltrialinstitutionmeetingtrial;
(9)Declarationthatthedevelopmentofinvestigationalmedicaldevicesmeetrelevantrequirementsofapplicablequalitymanagementsystemofmedicaldevices;
(10)Otherdocumentsrelatedtoethicalreview.
Ethicscommitteeshouldupholdtheprinciplesofethicsandscience,reviewandsupervisetheimplementationofclinicaltrials.
Article18Ifoneofthefollowingcasesoccurduringtheclinicaltrial,theinvestigatorshallreportintimetothemanagementdepartmentofmedicaldeviceclinicaltrialofclinicaltrialinstitution,informthesponsorandreporttheethicscommitteethroughthemanagementdepartment:
(1)Seriousadverseevents;
(2)Reportofprogress,includingsummaryforsafetyandreportofdeviation;
(3)Foranyrevisefortheapproveddocumentsbyethicscommittee,thenonsubstantivechangesthatdonotaffecttherightsandbenefits,safetyandhealthofsubjectsorisnotrelatedtothepurposeorendpointofclinicaltrialdon’tneedtobereportedinadvance,butshallbenotifiedinwrittenformafterwards.
(4)Suspension,terminationorrequiringforrestoringtheclinicaltrialaftersuspension;
(5)deviationofclinicaltrialprotocolaffectingtherightsandbenefits,safetyandhealthofsubjectsorthescientific nature.
Inordertoprotecttherightsandbenefits,safetyandhealthofsubjects,thedeviationinanemergencythatcan’tbereportedintimeshallbereportedassoonaspossibleinwrittenformafterwardsaccordingtorelevantprovisions.
Article19Intheprocessofclinicaltrial,inthecastthatrevisingtheclinicaltrialprotocol,informedconsentformandotherdocuments,requiringfordeviationandrestoringthesuspendedclinicaltrial,thetrialshallcontinuetobeimplementedafterbeingapprovedbytheethicscommittee.
Article20Theminors,pregnantwomen,oldpeople,personswithmentaldisability,patientsindangerandothersshallbeavoidedtobechosenassubjects;iftheyareneededtobechosenforsomenecessaryreason,relevantadditionalrequirementsprovidedbytheethicscommitteeshallbecompliedwith,andthespecialdesignshallbeconductedfortheirhealthconditionsintheclinicaltrialanditshallbehelpfultotheirhealth.
Article21Beforethesubjects’participatingintheclinicaltrial,theinvestigatorshallexplainthedetailsofclinicaltrialtothesubjects,the guardians of persons without or with limited capacity for civilconduct,includingrecognized,foreseeablerisksandpossibleadverseevents,etc.Thesubjectsandguardiansshallsigntheirnameandthedateontheinformedconsentformaftersufficientanddetainedexplanation,andtheinvestigatorshallalsoneedtosignhisnameandthedate.
Article22Thefollowingcontentsandexplanationso
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- 英文 医疗器械 临床试验 质量管理 规范
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