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该基础导论提供了安捷伦在药物开发中实施质量源于设计的解决方案的信息。
- Publication Part Number: 5991-2166CHCN
- Created: 14 Feb 2014
- 2 MB
色谱分析的样品前处理基本原理
- Publication Part Number: 5991-3326CHCN
- Created: 13 Nov 2013
- 17 MB
医薬品中の遺伝毒性不純物 レギュレーションと分析手法
- Publication Part Number: 5991-1876JAJP
- Created: 13 June 2013
- 2 MB
規制の適用を受ける製薬ラボにおける元素不純物分析
- Publication Part Number: 5991-0436JAJP
- Created: 30 Apr 2013
- 3 MB
药品中的遗传毒性杂质——法规和分析 基础导论
- Publication Part Number: 5991-1876CHCN
- Created: 21 Mar 2013
- 1 MB
バイオ医薬品ラボのコンプライアンス
- Publication Part Number: 5990-7001JAJP
- Created: 11 Feb 2013
- 1 MB
能源与化工行业分析仪解决方案指南 - 获得准确可靠的数据,确保高质高效的分析
- Publication Part Number: 5991-1561CHCN
- Created: 18 Dec 2012
- 12 MB
In this guide, we expand the GPC/SEC experiment by using additional detectors to deliver multi-detector or triple detection GPC/SEC
- Publication Part Number: 5990-7196RU
- Created: 16 Oct 2012
- 8 MB
法规制药实验室中的无机杂质分析基础导论
- Publication Part Number: 5991-0436CHCN
- Created: 04 July 2012
- 1 MB
在这本指南中,我们通过使用附加检测器将 GPC/SEC 实验扩展到了多检测器或三检测器 GPC/SEC。
- Publication Part Number: 5990-7196CHCN
- Created: 26 Apr 2012
- 3 MB
Pharmaceutical impurities are the unwanted chemicals that remain with active pharmaceutical ingredients (APIs) or drug product formulations.
- Publication Part Number: 5991-0090JAJP
- Created: 20 Apr 2012
- 2 MB
ISO/IEC 17025认证的理解与实施,作者 Ludwig Huber博士,旨在简要介绍ISO/IEC 17025认证:实验室认证的全球标准
- Publication Part Number: 5990-4540CHCN
- Created: 03 Sep 2009
- 7 MB
This new 84 page booklet from Agilent is a comprehensive guide to ICP-MS, designed to provide the reader with a clear understanding of the tecchnique ...
- Publication Part Number: 5989-3526CHCN
- Created: 01 June 2007
- 4 MB
- Publication Part Number: 5988-3921DEE
- Created: 21 Nov 2001
- 3 MB