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Primers
Portuguese version: Compliance By Design Primer (PDF)

Compliance by Design for Pharma QC Laboratories

  • Publication Part Number: 5991-5456PTBR
  • Created: 19 Mar 2015
  • 617 KB
  • PDF
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Primers
藥物質量控製實驗室的合規源於設計理念——來自 FDA 警告信的啟示 (PDF)

藥物質量控製實驗室的合規源於設計理念

  • Publication Part Number: 5991-5456CHCN
  • Created: 15 Jan 2015
  • 1 MB
  • PDF
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信心倍增——在藥物開發中實施質量源於設計的安捷倫解決方案 (PDF)

該基礎導論提供了安捷倫在藥物開發中實施質量源於設計的解決方案的信息。

  • Publication Part Number: 5991-2166CHCN
  • Created: 14 Feb 2014
  • 2 MB
  • PDF
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藥品中的遺傳毒性雜質——法規和分析 基礎導論 (PDF)

藥品中的遺傳毒性雜質——法規和分析 基礎導論

  • Publication Part Number: 5991-1876CHCN
  • Created: 21 Mar 2013
  • 1 MB
  • PDF
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Primers
Japanese version_Pharmaceutical Impurity Analysis Overview (PDF)

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
  • PDF
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Primers
German Version - Understanding and Implementing ISOIEC 17025 (PDF)

  • Created: 23 Nov 2009
  • 1 MB
  • PDF
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ISO/IEC 17025 認證的理解與實施 入門指南 (PDF)

ISO/IEC 17025認證的理解與實施,作者 Ludwig Huber博士,旨在簡要介紹ISO/IEC 17025認證：實驗室認證的全球標準

  • Publication Part Number: 5990-4540CHCN
  • Created: 03 Sep 2009
  • 7 MB
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