| Harmonization of strategies for the validation of quantitative analytical procedures: a SFSTP proposal—part I P Hubert, JJ Nguyen-Huu, B Boulanger, E Chapuzet, P Chiap, N Cohen, ... Journal of pharmaceutical and biomedical analysis 36 (3), 579-586, 2004 | 702 | 2004 |
| Compliance with antidepressants in a primary care setting, 1: beyond lack of efficacy and adverse events K Demyttenaere, P Enzlin, W Dewé, B Boulanger, J De Bie, W De Troyer, ... Journal of clinical psychiatry 62, 30-33, 2001 | 328 | 2001 |
| Analysis of recent pharmaceutical regulatory documents on analytical method validation E Rozet, A Ceccato, C Hubert, E Ziemons, R Oprean, S Rudaz, ... Journal of Chromatography A 1158 (1-2), 111-125, 2007 | 320 | 2007 |
| The SFSTP guide on the validation of chromatographic methods for drug bioanalysis: from the Washington Conference to the laboratory P Hubert, P Chiap, J Crommen, B Boulanger, E Chapuzet, N Mercier, ... Analytica Chimica Acta 391 (2), 135-148, 1999 | 308 | 1999 |
| Validation of quantitative analytical procedure, harmonization of approaches H Ph STP Pharma pratiques 13, 101-138, 2003 | 276* | 2003 |
| Design spaces for analytical methods E Rozet, P Lebrun, P Hubert, B Debrus, B Boulanger TrAC Trends in Analytical Chemistry 42, 157-167, 2013 | 270 | 2013 |
| Design space approach in the optimization of the spray-drying process P Lebrun, F Krier, J Mantanus, H Grohganz, M Yang, E Rozet, ... European Journal of Pharmaceutics and Biopharmaceutics 80 (1), 226-234, 2012 | 201 | 2012 |
| New advances in method validation and measurement uncertainty aimed at improving the quality of chemical data M Feinberg, B Boulanger, W Dewe, P Hubert Analytical and Bioanalytical chemistry 380, 502-514, 2004 | 200 | 2004 |
| An analysis of the SFSTP guide on validation of chromatographic bioanalytical methods: progresses and limitations B Boulanger, P Chiap, W Dewé, J Crommen, P Hubert Journal of pharmaceutical and biomedical analysis 32 (4-5), 753-765, 2003 | 186 | 2003 |
| Advances in validation, risk and uncertainty assessment of bioanalytical methods E Rozet, RD Marini, E Ziemons, B Boulanger, P Hubert Journal of pharmaceutical and biomedical analysis 55 (4), 848-858, 2011 | 184 | 2011 |
| Harmonization of strategies for the validation of quantitative analytical procedures: A SFSTP proposal: Part IV. Examples of application P Hubert, JJ Nguyen-Huu, B Boulanger, E Chapuzet, N Cohen, ... Journal of pharmaceutical and biomedical analysis 48 (3), 760-771, 2008 | 153 | 2008 |
| Towards a new age of virtual ADME/TOX and multidimensional drug discovery S Ekins, B Boulanger, PW Swaan, MAZ Hupcey Journal of computer-aided molecular design 16 (5), 381-401, 2002 | 137 | 2002 |
| Development of a new predictive modelling technique to find with confidence equivalence zone and design space of chromatographic analytical methods P Lebrun, B Govaerts, B Debrus, A Ceccato, G Caliaro, P Hubert, ... Chemometrics and Intelligent Laboratory Systems 91 (1), 4-16, 2008 | 115 | 2008 |
| Innovative high-performance liquid chromatography method development for the screening of 19 antimalarial drugs based on a generic approach, using design of experiments … B Debrus, P Lebrun, JM Kindenge, F Lecomte, A Ceccato, G Caliaro, ... Journal of Chromatography A 1218 (31), 5205-5215, 2011 | 112 | 2011 |
| Improvement of the decision efficiency of the accuracy profile by means of a desirability function for analytical methods validation: application to a diacetyl-monoxime … E Rozet, V Wascotte, N Lecouturier, V Préat, W Dewé, B Boulanger, ... Analytica chimica acta 591 (2), 239-247, 2007 | 108 | 2007 |
| Méthodes chromatographiques de dosage dans les milieux biologiques: stratégie de validation-Rapport d'une commission SFSTP E Chapuzet, N Mercier, S Bervoas-Martin, B Boulanger, P Chevalier, ... STP Pharma Pratiques 7 (3), 1997 | 106 | 1997 |
| Harmonization of strategies for the validation of quantitative analytical procedures-A SFSTP proposal-Part II H Ph, JJ Nguyen-Huu, B Boulanger, E Chapuzet, P Chiap, N Cohen, ... J Pharm Biomed Anal 45 (1), 70-81, 2007 | 101 | 2007 |
| Application of new methodologies based on design of experiments, independent component analysis and design space for robust optimization in liquid chromatography B Debrus, P Lebrun, A Ceccato, G Caliaro, E Rozet, I Nistor, R Oprean, ... Analytica Chimica Acta 691 (1-2), 33-42, 2011 | 99 | 2011 |
| Using tolerance intervals in pre-study validation of analytical methods to predict in-study results: The fit-for-future-purpose concept E Rozet, C Hubert, A Ceccato, W Dewé, E Ziemons, F Moonen, K Michail, ... Journal of Chromatography A 1158 (1-2), 126-137, 2007 | 88 | 2007 |
| Quality by design compliant analytical method validation E Rozet, E Ziemons, RD Marini, B Boulanger, P Hubert Analytical Chemistry 84 (1), 106-112, 2012 | 82 | 2012 |
Pierre LebrunUniversity of Liège, Pharmalex在 pharmalex.com 的电子邮件经过验证
