R. Klinkenberg

发表

Critical analysis of several analytical method validation strategies in the framework of the fit for purpose concept.

E. Chapuzet, A. Bouklouze, E. Rozet, 2010, Journal of chromatography. A.

Is supercritical fluid chromatography hyphenated to mass spectrometry suitable for the quality control of vitamin D3 oily formulations?

R. Marini, P. Hubert, É. Ziemons, 2017, Journal of chromatography. A.

Thorough characterization of a Self-Emulsifying Drug Delivery System with Raman hyperspectral imaging: a case study.

C. De Bleye, Pierre-François Chavez, P. Hubert, 2015, International journal of pharmaceutics.

An automated method for the simultaneous determination of pravastatin, 3-hydroxy isomeric metabolite, pravalactone and fenofibric acid in human plasma by sensitive liquid chromatography combined with diode array and tandem mass spectrometry detection.

B. Streel, B. Mertens, R. Klinkenberg, 2008, Journal of chromatography. A.

Moisture content determination of pharmaceutical pellets by near infrared spectroscopy: method development and validation.

J. Mantanus, P. Hubert, E. Rozet, 2009, Analytica chimica acta.

Development and validation of a liquid chromatographic method for the determination of amlodipine residues on manufacturing equipment surfaces.

A. Ceccato, B. Streel, A Ceccato, 2003, Journal of pharmaceutical and biomedical analysis.

A new criterion to assess distributional homogeneity in hyperspectral images of solid pharmaceutical dosage forms.

Eric Ziemons, Philippe Hubert, Eric Rozet, 2014, Analytica chimica acta.

Using total error concept for the validation of a liquid chromatography-tandem mass spectrometry method for the determination of budesonide epimers in human plasma.

B. Streel, R Klinkenberg, B Streel, 2009, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Sensitive determination of buprenorphine and its N-dealkylated metabolite norbuprenorphine in human plasma by liquid chromatography coupled to tandem mass spectrometry.

P. Hubert, A. Ceccato, B. Streel, 2003, Journal of pharmaceutical and biomedical analysis.

Validation of a liquid chromatographic-tandem mass spectrometric method for the determination of loperamide in human plasma.

P. Hubert, A. Ceccato, B. Streel, 2005, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Optimization and validation of a fast supercritical fluid chromatography method for the quantitative determination of vitamin D3 and its related impurities.

R. Marini, P. Hubert, É. Ziemons, 2017, Journal of chromatography. A.

Active content determination of non-coated pharmaceutical pellets by near infrared spectroscopy: method development, validation and reliability evaluation.

J. Mantanus, P. Hubert, E. Rozet, 2010, Talanta.

A new criterion to assess distributional homogeneity in hyperspectral images of solid pharmaceutical dosage forms.

C. De Bleye, Pierre-François Chavez, P. Hubert, 2014, Analytica chimica acta.

Critical analysis of several analytical method validation strategies in the framework of the fit for purpose concept.

P. Hubert, E. Rozet, É. Ziemons, 2010, Journal of chromatography. A.