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Understanding the impact of microcrystalline cellulose physicochemical properties on tabletability

International journal of pharmaceutics, 2015-07, Vol.490 (1-2), p.47-54

2015

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Analysis of recent pharmaceutical regulatory documents on analytical method validation

Journal of Chromatography A, 2007-07, Vol.1158 (1), p.111-125

2007

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Design space approach in the optimization of the spray-drying process

European journal of pharmaceutics and biopharmaceutics, 2012, Vol.80 (1), p.226-234

2012

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

Analytica chimica acta, 2014-03, Vol.818, p.7-14

2014

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Strategies for using the sheep ovarian cortex as a model in reproductive medicine

PloS one, 2014-03, Vol.9 (3), p.e91073-e91073

2014

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Application of new methodologies based on design of experiments, independent component analysis and design space for robust optimization in liquid chromatography

Analytica chimica acta, 2011-04, Vol.691 (1), p.33-42

2011

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PAT tools for the control of co-extrusion implants manufacturing process

International journal of pharmaceutics, 2013-12, Vol.458 (1), p.15-24

2013

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Validation of the Analytical Procedure for the Determination of Malondialdehyde and Three Other Aldehydes in Vegetable Oil Using Liquid Chromatography Coupled to Tandem Mass Spectrometry (LC-MS/MS) and Application to Linseed Oil

Food analytical methods, 2015-07, Vol.8 (6), p.1425-1435

2015

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

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2009-08, Vol.877 (23), p.2235-2243

2009

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Design Spaces for analytical methods

TrAC, Trends in analytical chemistry (Regular ed.), 2013-01, Vol.42, p.157-167

2013

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Validation of a method for the quantitation of ghrelin and unacylated ghrelin by HPLC

Journal of pharmaceutical and biomedical analysis, 2010-02, Vol.51 (3), p.633-639

2010

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Estimation of the Stability of Parathyroid Hormone when Stored at −80°C for a Long Period

Clinical journal of the American Society of Nephrology, 2009-12, Vol.4 (12), p.1988-1992

2009

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Analytical validation based on total error measurement and cut-off interpretation of a neonatal screening TSH-immunoassay

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2009-08, Vol.877 (23), p.2412-2417

2009

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Towards a full integration of optimization and validation phases: An analytical-quality-by-design approach

Journal of Chromatography A, 2015-05, Vol.1395, p.88-98

2015

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Laser-induced choroidal neovascularization model to study age-related macular degeneration in mice

Nature protocols, 2013-11, Vol.8 (11), p.2197-2211

2013

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Advances in validation, risk and uncertainty assessment of bioanalytical methods

Journal of pharmaceutical and biomedical analysis, 2011-06, Vol.55 (4), p.848-858

2011

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Compromise in uncertainty estimation by modelling and validation approaches for an HPLC-UV method for measurement of biochemical indicators of vitamins A and E

Analyst (London), 2018-03, Vol.143 (6), p.1492-151

2018

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Critical review of near-infrared spectroscopic methods validations in pharmaceutical applications

Journal of pharmaceutical and biomedical analysis, 2012-10, Vol.69, p.125-132

2012

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Robust method optimization strategy—A useful tool for method transfer: The case of SFC

Journal of pharmaceutical and biomedical analysis, 2014-01, Vol.88, p.519-524

2014

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Analytical validation of serum bone alkaline phosphatase (BAP OSTASE) on Liaison

Clinical chemistry and laboratory medicine, 2010-01, Vol.48 (1), p.67-72

2010

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Evaluation of the quantitative performances of supercritical fluid chromatography: From method development to validation

Journal of Chromatography A, 2014-08, Vol.1353, p.78-88

2014

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Harmonization of strategies for the validation of quantitative analytical procedures A SFSTP proposal. Part II

Journal of pharmaceutical and biomedical analysis, 2007-09, Vol.45 (1), p.70-81

2007

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Improvement of a stability-indicating method by Quality-by-Design versus Quality-by-Testing: A case of a learning process

Journal of pharmaceutical and biomedical analysis, 2014-01, Vol.88, p.401-409

2014

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Harmonization of strategies for the validation of quantitative analytical procedures A SFSTP proposal. Part III

Journal of pharmaceutical and biomedical analysis, 2007-09, Vol.45 (1), p.82-96

2007

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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 space

Journal of Chromatography A, 2011-08, Vol.1218 (31), p.5205-5215

2011

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Understanding the impact of microcrystalline cellulose physicochemical properties on tabletability

Analysis of recent pharmaceutical regulatory documents on analytical method validation

Design space approach in the optimization of the spray-drying process

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

Strategies for using the sheep ovarian cortex as a model in reproductive medicine

Application of new methodologies based on design of experiments, independent component analysis and design space for robust optimization in liquid chromatography

PAT tools for the control of co-extrusion implants manufacturing process

Validation of the Analytical Procedure for the Determination of Malondialdehyde and Three Other Aldehydes in Vegetable Oil Using Liquid Chromatography Coupled to Tandem Mass Spectrometry (LC-MS/MS) and Application to Linseed Oil

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

Design Spaces for analytical methods

Validation of a method for the quantitation of ghrelin and unacylated ghrelin by HPLC

Estimation of the Stability of Parathyroid Hormone when Stored at −80°C for a Long Period

Analytical validation based on total error measurement and cut-off interpretation of a neonatal screening TSH-immunoassay

Towards a full integration of optimization and validation phases: An analytical-quality-by-design approach

Laser-induced choroidal neovascularization model to study age-related macular degeneration in mice

Advances in validation, risk and uncertainty assessment of bioanalytical methods

Compromise in uncertainty estimation by modelling and validation approaches for an HPLC-UV method for measurement of biochemical indicators of vitamins A and E

Critical review of near-infrared spectroscopic methods validations in pharmaceutical applications

Robust method optimization strategy—A useful tool for method transfer: The case of SFC

Analytical validation of serum bone alkaline phosphatase (BAP OSTASE) on Liaison

Evaluation of the quantitative performances of supercritical fluid chromatography: From method development to validation

Harmonization of strategies for the validation of quantitative analytical procedures A SFSTP proposal. Part II

Improvement of a stability-indicating method by Quality-by-Design versus Quality-by-Testing: A case of a learning process

Harmonization of strategies for the validation of quantitative analytical procedures A SFSTP proposal. Part III

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 space

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