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时间:2018-04-16
《翻译(supac-ir指导原则速释口服固体制剂放大生产和批准后变更)》由会员上传分享,免费在线阅读,更多相关内容在应用文档-天天文库。
1、GuidanceforIndustryImmediateReleaseSolidOralDosageFormsScale-UpandPostapprovalChanges:Chemistry,Manufacturing,andControls,InVitroDissolutionTesting,andInVivoBioequivalenceDocumentationSUPAC-IR指导原则:速释口服固体制剂放大生产和批准后变更:化学、生产和控制,体外溶出试验、体内生物等效性文件CenterforDrugEvaluationandResearch(CDER)November1995CMC
2、5药品评价与研究中心1995年11月CMC5TABLEOFCONTENTS目录I.PURPOSEOFGUIDANCE(本指导原则的目的)......................................1II.DEFINITIONOFTERMS(术语定义)...............................................3III.COMPONENTSANDCOMPOSITION(辅料成分或组成的变更)..........................6IV.SITECHANGES(地点变更)............................
3、..........................13V.CHANGESINBATCHSIZE(SCALE-UP/SCALE-DOWN)(批量大小(放大/缩小)的变更)......16VI.MANUFACTURING(生产变更)...................................................18VII.INVITRODISSOLUTION(体外溶出试验)..........................................23VIII.INVIVOBIOEQUIVALENCESTUDIES(体内生物等效性).............
4、................23IX.REFERENCES(参考文献)......................................................25APPENDIXA:NARROWTHERAPEUTICRANGEDRUGS(附录A:治疗窗狭窄药物).........A-1GUIDANCEFORINDUSTRY1IMMEDIATERELEASESOLIDORALDOSAGEFORMSSCALE-UPANDPOSTAPPROVALCHANGES:CHEMISTRY,MANUFACTURING,ANDCONTROLS,INVITRODISSOLUTION
5、TESTING,ANDINVIVOBIOEQUIVALENCEDOCUMENTATION速释口服固体制剂放大生产和批准后变更:化学、生产和控制,体外溶出试验、体内生物等效性文件I.PURPOSEOFGUIDANCE(本指导原则的目的)Thisguidanceprovidesrecommendationstosponsorsofnewdrugapplications(NDA's),abbreviatednewdrugapplications(ANDA's),andabbreviatedantibioticapplications(AADA's)whointend,duringthepos
6、tapprovalperiod,tochange:1)thecomponentsorcomposition;2)thesiteofmanufacture;3)thescale-up/scale-downofmanufacture;and/or4)themanufacturing(processandequipment)ofanimmediatereleaseoralformulation.本指导原则所提供的的建议适用于新药申请(NDA's)、仿制药申请(ANDA's)和抗生素仿制药申请(AANA’S)的企业的批准后变更,内容包括:1)成分或组分的变更;2)生产地点的变更;3)放大/缩小
7、生产规模的变更;和/或4)生产过程(工艺和设备)的变更Thisguidanceistheresultof:1)aworkshoponthescale-upofimmediatereleasedrugproductsconductedbytheAmericanAssociationofPharmaceuticalScientistsinconjunctionwiththeUnitedStatesPharmacopoeialConventionan
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