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Showing results (51-60 of 62) with videos related to

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Journal of Pharmaceutical and Biomedical Analysis|August 6, 2013
Application of an innovative design space optimization strategy to the development of LC methods for the simultaneous screening of antibiotics to combat poor quality medicinesJ K Mbinze, A Dispas, P Lebrun, et al.
Journal of Pharmaceutical and Biomedical Analysis|October 3, 2006
Robustness testing of a chiral NACE method for R-timolol determination in S-timolol maleate and uncertainty assessment from quantitative dataR D Marini, E Rozet, Y Vander Heyden, et al.
Analytica Chimica Acta|January 17, 2012
Usefulness of capability indices in the framework of analytical methods validationA Bouabidi, E Ziemons, R Marini, et al.
Journal of Pharmaceutical and Biomedical Analysis|December 23, 2019
Performance evaluation of a MIP for the MISPE-LC determination of p-[<sup>18</sup>F]MPPF and a potential metabolite in human plasmaF Lecomte, J Aerts, A Plenevaux, et al.
Journal of Pharmaceutical and Biomedical Analysis|August 20, 2010
Reliable low-cost capillary electrophoresis device for drug quality control and counterfeit medicinesR D Marini, E Rozet, M L A Montes, et al.
Journal of Chromatography. A|June 28, 2011
Innovative high-performance liquid chromatography method development for the screening of 19 antimalarial drugs based on a generic approach, using design of experiments, independent component analysis and design spaceB Debrus, P Lebrun, J Mbinze Kindenge, et al.
Journal of Chromatography. A|September 8, 2009
Critical analysis of several analytical method validation strategies in the framework of the fit for purpose conceptA Bouabidi, E Rozet, M Fillet, et al.
Journal of Chromatography. A|October 11, 2012
Application of an innovative design space optimization strategy to the development of liquid chromatographic methods to combat potentially counterfeit nonsteroidal anti-inflammatory drugsJ K Mbinze, P Lebrun, B Debrus, et al.
Journal of Pharmaceutical and Biomedical Analysis|September 5, 2008
Harmonization of strategies for the validation of quantitative analytical procedures: a SFSTP proposal part IV. Examples of applicationPh Hubert, J-J Nguyen-Huu, B Boulanger, et al.
Journal of Pharmaceutical and Biomedical Analysis|August 25, 2007
Harmonization of strategies for the validation of quantitative analytical procedures. A SFSTP proposal--part IIIPh Hubert, J-J Nguyen-Huu, B Boulanger, et al.
Pageof 7

Showing results (51-60 of 62) with videos related to

Sort By:
Pageof 7
Journal of Pharmaceutical and Biomedical Analysis|August 6, 2013
Application of an innovative design space optimization strategy to the development of LC methods for the simultaneous screening of antibiotics to combat poor quality medicinesJ K Mbinze, A Dispas, P Lebrun, et al.
Journal of Pharmaceutical and Biomedical Analysis|October 3, 2006
Robustness testing of a chiral NACE method for R-timolol determination in S-timolol maleate and uncertainty assessment from quantitative dataR D Marini, E Rozet, Y Vander Heyden, et al.
Analytica Chimica Acta|January 17, 2012
Usefulness of capability indices in the framework of analytical methods validationA Bouabidi, E Ziemons, R Marini, et al.
Journal of Pharmaceutical and Biomedical Analysis|December 23, 2019
Performance evaluation of a MIP for the MISPE-LC determination of p-[<sup>18</sup>F]MPPF and a potential metabolite in human plasmaF Lecomte, J Aerts, A Plenevaux, et al.
Journal of Pharmaceutical and Biomedical Analysis|August 20, 2010
Reliable low-cost capillary electrophoresis device for drug quality control and counterfeit medicinesR D Marini, E Rozet, M L A Montes, et al.
Journal of Chromatography. A|June 28, 2011
Innovative high-performance liquid chromatography method development for the screening of 19 antimalarial drugs based on a generic approach, using design of experiments, independent component analysis and design spaceB Debrus, P Lebrun, J Mbinze Kindenge, et al.
Journal of Chromatography. A|September 8, 2009
Critical analysis of several analytical method validation strategies in the framework of the fit for purpose conceptA Bouabidi, E Rozet, M Fillet, et al.
Journal of Chromatography. A|October 11, 2012
Application of an innovative design space optimization strategy to the development of liquid chromatographic methods to combat potentially counterfeit nonsteroidal anti-inflammatory drugsJ K Mbinze, P Lebrun, B Debrus, et al.
Journal of Pharmaceutical and Biomedical Analysis|September 5, 2008
Harmonization of strategies for the validation of quantitative analytical procedures: a SFSTP proposal part IV. Examples of applicationPh Hubert, J-J Nguyen-Huu, B Boulanger, et al.
Journal of Pharmaceutical and Biomedical Analysis|August 25, 2007
Harmonization of strategies for the validation of quantitative analytical procedures. A SFSTP proposal--part IIIPh Hubert, J-J Nguyen-Huu, B Boulanger, et al.
Pageof 7