Literature DB >> 18170982

Determination of carryover and contamination for mass spectrometry-based chromatographic assays.

Nicola C Hughes1, Ernest Y K Wong, Juan Fan, Navgeet Bajaj.   

Abstract

The Third American Association of Pharmaceutical Scientists/Food and Drug Administration Bioanalytical Workshop, held in 2006, reviewed and evaluated current practices and proposed that carryover and contamination be assessed not only during the validation of an assay but also during the application of the method in a study. In this article, the potential risks of carryover and contamination in each stage of a bioanalytical method are discussed, to explain to the industry why this recommendation is being made.

Mesh：

Year:  2007        PMID： 18170982      PMCID： PMC2751487          DOI： 10.1208/aapsj0903042

Source DB:  PubMed          Journal:  AAPS J        ISSN： 1550-7416            Impact factor:   4.009


  8 in total

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  8 in total
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