961, 2011, annex 7 WHO 药品生产技术转移的指导原则 1 of 32 © World Health Organization 世界卫生组织 WHO Technical Report Series, No. 961, 2011 世界卫生组织技术报告系列,编号 961, 2011 年 Annex 7 附录 7 WHO guidelines on transfer of technology in pharmaceutical manufacturing WHO 药品生产技术...
Validation of heating, ventilation and air-conditioning systems (as cross-reference to TRS 1010, Annex 8 (4))■ Appendix 2. Validation of water systems for pharmaceutical use (as published in TRS 937, Annex 4, 2006 and as cross-reference to TRS 970, Annex 2, 2012(5)■ Appendix 3. ...
Note: For details on cleaning validation, see WHO Technical Report Series, No. 1019, Annex 3, Appendix 3, 2019 and the WHO Points to consider when including HBELs in cleaning validation, TRS XXX, Annex 2, 2021. 注意:有关清洁...
WHO_TRS_961-Annex 3 WHO GMP for pharmaceutical products-main principles 星级: 66 页 WHO_TRS_961_annex 7 cold chain 星级: 25 页 WHO_TRS_961Annex9 补充文件10-温度监控装置准确度检查_中英文_完 星级: 36 页 who_trs_908-annex9 星级: 12 页 WHO_TRS_908-Annex9 星级: 12 页 who...
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Annex5 Guidanceongooddataandrecordmanagementpractices Background Duringaninformalconsultationoninspection,goodmanufacturingpractices andriskmanagementguidanceinmedicines’manufacturingheldbythe WorldHealthOrganization(WHO)inGenevainApril2014,aproposalfor newguidanceongooddatamanagementwasdiscussedanditsdevelopment ...
1019,Annex 3, Appendix 3, 2019 and the WHO Points to consider when including HBELsin cleaning validation, TRS XXX, Annex 2, 2021. 注:有关清洁验证的详细信息,请参阅WHO技术报告系列第1019号,附录3,2019和WHO《清洁验证中应用HBEL的考量》,TRS XXX,附录2,2021。 22.1. Research and development ...
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中英文对照的和原文，请忽略前一份。
1019,Annex 3, Appendix 3, 2019 and the WHO Points to consider when including HBELsin cleaning validation, TRS XXX, Annex 2, 2021. 注:有关清洁验证的详细信息,请参阅WHO技术报告系列第1019号,附录3,2019和WHO《清洁验证中应用HBEL的考量》,TRS XXX,附录2,2021。 22.1. Research and development ...