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Development and validation of a sensitive solid phase extraction/hydrophilic interaction liquid chromatography/mass spectrometry method for the accurate determination of glucosamine in dog plasma.


C. Hubert, S. Houari, F. Lecomte, V. Houbart, C. De Bleye, M. Fillet, G. Piel, E. Rozet, Ph. Hubert
Journal of Chromatography A, Volume 1217, Issue 19, 7 May 2010, Pages 3275-3281...

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Enantiomeric purity testing of S-timolol by non-aqueous CE using heptakis(2,3-di-O-methyl-6-O-Sulfo)-?-cyclodextrin as chiral additive – Validation using the accuracy profile strategy and estimation of uncertainty


Marini Djang''Eing''A, Roland Servais, Anne-Catherine; Rozet, Eric et al
31st International Symposium on HPLC and Related techniques
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Harmonization of strategies for the validation of quantitative analytical procedures. A SFSTP proposal--part III.


Ph. Hubert, J.-J. Nguyen-Huu, B. Boulanger, E. Chapuzet, N. Cohen, P.-A. Compagnon, W. Dewé, M. Feinberg, M. Laurentie, N. Mercier, G. Muzard, L. Valat, E. Rozet
Journal of...

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Optimisation and validation of a fast HPLC method for the quantification of sulindac and its related impurities


Krier F., Brion M., Debrus B., Lebrun P., Driesen A., Ziemons E., Evrard B., Hubert P.
Journal of pharmaceutical and biomedical analysis, volume 54, issue 4, 25 march 2011, pages...

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A fast ultra-high pressure liquid chromatographic method for qualification and quantification of pharmaceutical combination preparations containing paracetamol, acetyl salicylic acid and/or antihistaminics


Deconinck E., Sacré P.Y., Baudewyns S., Courselle P., De Beer J.
Journal of Pharmaceutical and Biomedical Analysis, volume 56, issue 2, 10 septembre 2011, pages 200-209
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A global approach to method validation and measurement uncertainty


Feinberg M., Laurentie M.
Accreditation and Quality Assurance, volume 11, issue 1-2, 28 january 2006, pages 3-9
 

A new validation approach applied to the GC determination of impurities in organic solvents


Jacobs P., Dewé W., Flament A., Gibella M., Ceccato A.
Journal of Pharmaceutical and biomedical Analysis, volume 40, issue 2, 13 february 2006, pages 294-304
 

A practical guide to analytical method validation, including measurement uncertainty and accuracy profiles


Gustavo Gonzalez A., Angeles Herrador M.
Trends in Analytical Chemistry, Volume 26, issue 3, March 2007, pages 227-238
 

A preliminary evaluation of dexamethasone palmitate emulsion: a novel intravitreal sustained delivery of corticosteroid for treatment of macular edema


Daull P., Paterson C.A., Kuppermann B.D., Garigue J.S.
The journal of ocular pharmacology and therapeutics (epub 2013 january 18)
 

A risk-based analysis of the AAPS conference report on quantitative bioanalytical methods validation and implementation


Bruno Boulanger, Eric Rozet, François Moonen, Serge Rudaz, Philippe Hubert
Journal of Chromatography B, Volume 877, Issue 23, 1 August 2009, Pages 2235-2243
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A validated method for the quantification of pimarane and trachylobane diterpenes in the leaves of Croton Zambesicus by capillary gas chromatography


S. BLOCK, D. BRKIC, Ph. HUBERT et J. QUETIN-LECLERCQ.
Phytochem Anal. 2005 Sep-Oct;16(5):342-8.
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A validated ultra-high pressure liquid chromatographic method for the characterisation of confiscated illegal slimming products containing anorexics


Deconinck E., Verlinde K., Courselle P., Beer J.O.
Journal of Pharmaceutical and biomedical analysis, volume 59, 5 February 2012, pages 38-43
 

Accuracy profile theory for the validation of an LC-MS-MS method for the determination of Risperidone and 9-Hydroxyrisperidone in human Plasma


Xianhua Zhang, Xia Zhao, Chao Zhang, Li Yang, Xin Xiong, Yong Zhou, Yiheng Yang, Jingli Duan
Chromatographia, volume 71, 2010 april 24, pages 1015-1023
 

Accuracy profile validation of a new method for carbon monoxide measurement in the human blood using headspace-gas chromatography-mass spectrometry (HS-GC-MS)

Varlet V., Lagroy de Croutte E., Augsburger M., Manguin P.
Journal of Chromatography B, volume 880, 1 Jan 2012, pages 125-131
 

Accuracy Profiles from uncertainty measurements


Gustavo Gonzalez A., Angeles Herrador M.
Talanta, volume 70, issue 4, 15 November 2006, pages 896-901
 

Acetominophen determination in low-dose pharmaceutical syrup by NIR spectroscopy


Ziemons, Eric; Mantanus, Jérôme; Lebrun, Pierre et al
in Journal of Pharmaceutical & Biomedical Analysis (2010), 53
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Active content determination of non-coated pharmaceutical pellets by near infrared spectroscopy: Method development, validation and reliability evaluation


J. Mantanus, E. Ziémons, P. Lebrun, E. Rozet, R. Klinkenberg, B. Streel, B. Evrard, Ph. Hubert
Talanta, Volume 80, Issue 5, 15 March 2010, Pages 1750-1757
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Advances in validation, risk and uncertainty assessment of bioanalytical methods


Rozet E, Marini R.D., Ziemons E., Boulanger B., Hubert Ph.
Journal of Pharmaceutical and Biomedical Analysis, volume 55, issue 4, 25 june 2011, pages 848-858
 

An Analysis of Recent Pharmaceutical Regulatory Documents on Analytical Method Validation


ROZET E., CECCATO A., HUBERT C., ZIEMONS E., OPREAN R., RUDAZ S., BOULANGER B., HUBERT P.
J. Chrom A, volume 1158, 2007 , 111-125
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An analysis of the SFSTP guide on validation of chromatographic bioanalytical methods: progresses and limitations


B. Boulanger, P. Chiap, W. Dewe, J. Crommen, Ph. Hubert
Journal of Pharmaceutical and Biomedical Analysis, Volume 32, Issues 4-5, 8 August 2003, Pages 753-765
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