Plate Number Requirements for Establishing Method Suitability

Establishing the suitability of an analytical system has become a routine requirement in the testing of modern pharmaceuticals. Acceptable parameters that illustrate the system is performing as intended and in an equivalent manner to the original validation are often set at the time of method valida...

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Bibliographic Details
Published inJournal of chromatographic science Vol. 43; no. 2; pp. 67 - 72
Main Authors Webster, Gregory K., Diaz, Angel R., Seibert, Donna S., Weekley, Brian S., Jackson, J. Derek
Format Journal Article
LanguageEnglish
Published Niles, IL Oxford University Press 01.02.2005
Preston Publications
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Summary:Establishing the suitability of an analytical system has become a routine requirement in the testing of modern pharmaceuticals. Acceptable parameters that illustrate the system is performing as intended and in an equivalent manner to the original validation are often set at the time of method validation and transferred with the method to the production laboratory. For chromatographic methods, these parameters include—but are not limited to—resolution, tailing, and plate number specifications. Transferring methods is often a seamless transition from research to quality control. However, far too often the quality group receives arguably “overzealous” and strict requirements for the method. More specifically, chromatographic methods get issued with plate number specifications that far exceed the minimum number required to achieve sufficient resolution of the analytes. Presented here is a discussion of the setting of realistic plate number specifications that still maintain the minimum resolution of the chromatographic critical pair.
Bibliography:ark:/67375/HXZ-C65G9MTP-6
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ObjectType-Article-1
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content type line 23
ISSN:0021-9665
1945-239X
DOI:10.1093/chromsci/43.2.67