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ICH H H M7M7指南在原EDQM料药在原认证EP料药认证ED应用认证EPQM CEP认证中的应用

2016年 第02月 04 | 浙江海翔药业药业股份有限公司,浙,浙台州1800台州 318台州台州 300 318000

摘 要:介绍了在原料药E原料药ECEP认DQM DQM DQM CEP认证时,如证时,如证时,如何应用ICH M7对原料,包括D药进行D药进行D性杂质的NA诱变的制定以估并控制性风险评及质量控,包括D性杂质的NA诱变及质量控确定、可确定、可接受限度性杂质的估并控制,包括DNA诱变性杂质的确定、可接受限度的制定以及质量控制等。

【分 类】 【医药、卫生】 > 药学 > 药事组织【经济】 > 工业经济 > 中国工业经济 > 工业部门经济【经济】 > 经济计划与管理 > 国民经济管理 > 生产行业管理
【关键词】 DNA诱变性 基因毒性 原料药
【出 处】 2016年 第02月 04 181-182页 共2页
【收 录】 中文科技期刊数据库

【参考文献】
[1]ICH[1]ICH Expert Wingorkt Wingingorksseent Grentssesse. A aneacssming Gr. Anictive (entsseontroloup. Aentssessmtivent an Pol Cd Contin rol ofgenk,S Lipurtiv to14.tivk,Ses DNpuralsceuA RperrmaeacoupMut to Gr)Imtiv)Ime (Mut Ask,Sagenic)Impurperiti Lies in c) 4.PhantrPhaRisarcrma Li 4.andeutceuticalsinols mitper toiveten LiICHingtia Extenl Cmit2.Ic R Potent Wtiatial Cmack,Sarcddeinogengenic m tRishark,Stepiskdde 4.eni New DsesoupICH(Mu2.In PICH]IC IC,2014.[2]uri IC]ICingc) CH,rug Q3 Q3ICH201 ExGuiper006t Writs, duanog)Stol orking GrLimdelesiouprt IC2.I. Ac) ol ls bstH Eivenogddeddec Rndum t,Tao ICH M7:ial Asrcieliep ertto ilisesExpkinpurExpsmert nt harand Contr5:1ol sa rouof entDNA Reg GactineCecivea(R(MutagWoreni232c Rc) Impuritiebst(R5e,Eeniiesicas in Phar006se 200linnogmaceuticals es:to Limritl S)Stsa it Pot MuogeH Eignent2.Iial Catia/CHmpurcinogenic Riskc I,M7(R1 ImQ3c4/22.Ip.I4]I]Gu(R5)St2)Sng ep ova2.IsioineWor:1-tre5:1eniCH,y a201xic5:1 BeBos006s, e,Ees'H,2nig[7]Guirug of.[3H Ev.3]IC41 genH Expert Working Gcin8:2. Eroup.I6.4/2mpu:7.134MP/ritCH ine. Eropiesdua inTox200mpu134 New Dersertrugign Su-aMa JedibstNetancershe otoes, Q3stiAgeew a(R2)Step 4. ICa BH,211:ertrit006 Rele :1-5.[4]Iof 431CH ExpNetdo ert Worki]GuGroforualng Group. ImazkAgeilient0:2forEurpur6.16.ities:GuidelrulineLim0:2 foEurr Residuaityl Solvents, Q3c(R5)Step ni/4. dely aICH200n, ,20ies imlinpeanotdo 41 11:ncy15-16.[5]Romualdo CHMBenoduignebaa, noti, MP/Cecilia Bossn, a, WorNina Jeliazke lediova,Tatia/ 2peaope41 na Netzevaand Andrew Worgenth.MEA, EonsThe Beeninigni/Bossa tagrulebase for Muidee ltagenile citcy,y asiond Carcinogenicity-aModuonsEurle of Guian Tox/25he tree,EUR 232 an41 EN–9942008. European Commission, c I2008:2-12.[6]Guideline lMP/MP/e on t:7.he Limeanits of GenotMP/oxic I.Eumpurities, EMEAedi/CHMP/ Me201QWP/251344/2006. European Medicines Agency, 2006dic:7.[7]Questions and answers ondic the 'GuidelinegenCHM on th ime limi.Euts of genotoxic impurities', EMA/CHMP/SWP/v.3431994/ 2007ine Rev.3.European Medicines Agen0:2cy,2010:2,5-6.

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来源期刊
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