A Validation Process for Data from the Analysis of Drugs in Biological Fluids-Reference-Cited by-同舟云学术

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A Validation Process for Data from the Analysis of Drugs in Biological Fluids

Published:1985-01 Issue:9-10 Volume:11 Page:1703-1728
ISSN:0363-9045
Container-title:Drug Development and Industrial Pharmacy
language:en
Short-container-title:Drug Development and Industrial Pharmacy

Author:

Brooks Marvin A.,Weinfeld Robert E.

Publisher

Informa UK Limited

Subject

Organic Chemistry,Drug Discovery,Pharmaceutical Science,Pharmacology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03639048509057695

Reference1 articles.

1. Determination of cibenzoline in plasma and urine by high-performance liquid chromatography

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1. The physicochemical characteristics and bioavailability of indomethacin from β-cyclodextrin, hydroxyethyl-β-cyclodextrin, and hydroxypropyl-β-cyclodextrin complexes;International Journal of Pharmaceutics;2004-02

2. Validation of bioanalytical chromatographic methods;Journal of Pharmaceutical and Biomedical Analysis;1998-06

3. Drug analysis of biological samples. A survey of validation approaches in chromatography in the UK pharmaceutical industry;Xenobiotica;1992-01

4. Liquid chromatographic methods validation for pharmaceutical products;Journal of Pharmaceutical and Biomedical Analysis;1990-01

5. Toxicity, pharmacokinetics and metabolism of iododoxorubicin in cancer patients;European Journal of Cancer and Clinical Oncology;1990-01

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