Enhancing drug development by applying LC-MS-MS for cleaning validation in manufacturing equipment: LC-MS-MS has the potential to become a routine technique for determining drug residues in support of cleaning verification, especially early in drug development

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Bibliographic Details
Published in:Pharmaceutical technology (2003) 2006-02, Vol.30 (2), p.56
Main Authors: Kolodsick, Kevin J, Phillips, Holly, Feng, Jennifer, Molski, Matthew, Kingsmill, Carol A
Format: Magazinearticle
Language:English
Subjects:
Drugs
Liquid chromatography
Mass spectrometry
Pharmaceutical industry
Product development
Production processes
Quality management
Technology application
Online Access:Get full text
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ISSN:1543-2521