An alternative solution to overcome carryover issues in bioanalysis.
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Fabio Garofolo | Louis-Philippe Morin | Milton Furtado | Marie-Pierre Taillon | Milton Furtado | F. Garofolo | Louis-Philippe Morin | M. Taillon
[1] Naidong Weng,et al. Systematic troubleshooting for LC/MS/MS. Part 2: Large-scale LC/MS/MS and automation , 2002 .
[2] E. Woolf,et al. Elimination of autosampler carryover in a bioanalytical HPLC-MS/MS method: a case study. , 2005, Journal of pharmaceutical and biomedical analysis.
[3] Eric Woolf,et al. 2010 white paper on recent issues in regulated bioanalysis & global harmonization of bioanalytical guidance. , 2010, Bioanalysis.
[4] Chung Chow Chan,et al. Analytical Method Validation and Instrument Performance Verification , 2011 .
[5] Roger Hayes,et al. Recommendations on: internal standard criteria, stability, incurred sample reanalysis and recent 483s by the Global CRO Council for Bioanalysis. , 2011, Bioanalysis.
[6] Nicola C Hughes,et al. Determination of carryover and contamination for mass spectrometry-based chromatographic assays , 2007, The AAPS Journal.
[7] Xia Yin,et al. 2009 White Paper on recent issues in regulated bioanalysis from the 3rd Calibration and Validation Group Workshop. , 2010, Bioanalysis.
[8] D. S. Hage,et al. System suitability in bioanalytical LC/MS/MS. , 2007, Journal of pharmaceutical and biomedical analysis.
[9] Fabio Garofolo,et al. The 2nd Calibration and Validation Group workshop on recent issues in good laboratory practice bioanalysis. , 2009, Bioanalysis.
[10] Fabio Garofolo,et al. Bioanalytical Method Validation , 2004 .