The importance of impurity analysis in pharmaceutical products: an integrated approach-Reference-Cited by-同舟云学术

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The importance of impurity analysis in pharmaceutical products: an integrated approach

Published:2006-03-09 Issue:1-2 Volume:11 Page:69-74
ISSN:0949-1775
Container-title:Accreditation and Quality Assurance
language:en
Short-container-title:Accred Qual Assur

Author:

Rahman Nafisur,Azmi Syed Najmul Hejaz,Wu Hui-Fen

Publisher

Springer Science and Business Media LLC

Subject

Safety, Risk, Reliability and Quality,Instrumentation,General Chemical Engineering,General Chemistry

Link

http://link.springer.com/content/pdf/10.1007/s00769-006-0095-y.pdf

Reference35 articles.

1. Barber HJ (1978) Historical aspects of chemotherapy. May and Baker Ltd., Dagenham, UK

2. De Quincey T (1972) Confessions of an English opium-eater. Dent TM and Sons Ltd., London

3. International Conference on Harmonisation, ICH (1997) Q3C Impurities: residual solvents, USA

4. International Conference on Harmonisation, ICH (2003) Q1A (R2) Stability testing of new drug substances and products, USA

5. International Conference on Harmonisation, ICH (2000) Analytical procedures and methods validation, USA

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