INTERNATIONALCONFERENCEONHARMONISATIONOFTECHNICALREQUIREMENTSFORREGISTRATIONOFPHARMACEUTICALSFORHUMANUSEICHHARMONISEDTRIPARTITEGUIDELINEGOODMANUFACTURINGPRACTICEGUIDEFORACTIVEPHARMACEUTICALINGREDIENTSQ7CurrentStep4versiondated10November2000ThisGuidelinehasbeendevelopedbytheappropriateICHExpertWorkingGroupandhasbeensubjecttoconsultationbytheregulatoryparties,,,(s)(SelfInspection)(自检),Intermediates,、中间体、(主生产和控制记录)(MasterProductionandControlRecords)(批生产和控制记录)(BatchProductionandControlRecords)--
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