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BIS repetita non placent—a statistical analysis of the number of sample preparations and number of injections required for chromatographic analyses

Journal of pharmaceutical and biomedical analysis, 2005-02, Vol.37 (2), p.313-318

2005

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Application of a modified central composite design to optimize the capillary electrochromatographic separation of related S-oxidation compounds

Journal of Chromatography A, 1997-05, Vol.769 (2), p.145-153

1997

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Determination of a novel bile acid sequestrant in rodent diet by near-infrared spectroscopy

Journal of pharmaceutical and biomedical analysis, 1999-05, Vol.19 (6), p.903-910

1999

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Capillary Electrochromatography as a Method Development Tool for the Liquid Chromatographic Separation of DUP 654 and Related Substances

Journal of high resolution chromatography, 1998-03, Vol.21 (3), p.161-168

1998

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Process and Method Variability Modeling to Achieve QbD Targets

AAPS PharmSciTech, 2016-04, Vol.17 (2), p.523-527

2016

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Meeting Report: Vaccine Stability Considerations to Enable Rapid Development and Deployment

AAPS open, 2021-12, Vol.7 (1), p.6-6, Article 6

2021

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Dissolution Best Practices and International Harmonization - AAPS Workshop Report

Dissolution technologies, 2022-11, Vol.29 (4), p.230-236

2022

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Multifactor Non-linear Modelling for Accelerated Stability Analysis and Prediction

Pharmaceutical technology Europe, 2014-07, Vol.26 (7), p.36

2014

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Multifactor non-linear modelling for accelerated stability analysis and prediction: the right approach can provide a clear, statistically defendable method for determining dissolution and accelerated stability

Pharmaceutical technology Europe, 2014-07, Vol.26 (7), p.36

2014

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Strategies of Bringing Drug Product Marketing Applications to Meet Current Regulatory Standards

AAPS PharmSciTech, 2015-08, Vol.16 (4), p.986-991

2015

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Method validation by design to support formulation development

Pharmaceutical technology Europe, 2013-04, Vol.25 (4), p.48

2013

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Separation of diastereoisomers of DuP 105, a novel oxazolidinone antibacterial agent, by supercritical fluid chromatography on a Chiralcel OD column

Journal of pharmaceutical and biomedical analysis, 1996-05, Vol.14 (7), p.807-814

Alasandro, Mark

1996

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Early Development GMPs for stability: an industry perspective (Part IV)

Pharmaceutical technology Europe, 2012-10, Vol.24 (10), p.61

2012

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Investigation of pharmaceutical high-performance liquid chromatography assay bias using experimental design

Journal of Chromatography A, 2001-05, Vol.917 (1), p.63-73

2001

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Multifactor Non-linear Modeling for Accelerated Stability Analysis and Prediction

Pharmaceutical Technology, 2014-07, Vol.38 (7), p.46

2014

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Degradation of a Fluoropyridinyl Drug in capsule Formulation: Degradant Identification, Proposed Degradation Mechanism, and Formulation Optimization

Pharmaceutical development and technology, 2000, Vol.5 (4), p.561-570

2000

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Microcolumn liquid chromatography of benzoyl derivatives of steroid metabolites

Analytical chemistry (Washington), 1983-12, Vol.55 (14), p.2375-2377

1983

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New biochemical separations using precolumn derivatization and microcolumn liquid chromatography

Journal of Chromatography A, 1984-05, Vol.292 (1), p.159-167

1984

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Quantitative alterations of steroid urinary profiles associated with diabetes mellitus

Clinica chimica acta, 1982-12, Vol.126 (3), p.243-255

1982

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STEROID PROFILING STUDIES OF DIABETES MELLITUS AND THE HISTOCOMPATIBILITY-2 COMPLEX OF THE MOUSE THROUGH CHROMATOGRAPHIC METHODS (CAPILLARY GC, MICROCOLUMN LC, ANIMAL MODELS)

ALASANDRO, MARK STEPHEN

1984

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Early Development GMPs for Stability

Pharmaceutical Technology, 2012-09, Vol.36 (9), p.64

2012

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Identification of out-of-trend stability results

Pharmaceutical Technology, 2003-04, Vol.27 (4), p.38

2003

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Method validation by design to support formulation development

Pharmaceutical Technology, 2013-04, Vol.37 (4), p.84

2013

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Multifactor non-linear modeling for accelerated stability analysis and prediction: the right approach can provide a clear, statistically defendable method for determining dissolution and accelerated stability

Pharmaceutical technology (2003), 2014-07, Vol.38 (7), p.46

2014

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Identification of out-of-trend stability results, Part II

Pharmaceutical Technology, 2005-10, Vol.29 (10), p.66-78

2005

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BIS repetita non placent—a statistical analysis of the number of sample preparations and number of injections required for chromatographic analyses

Application of a modified central composite design to optimize the capillary electrochromatographic separation of related S-oxidation compounds

Determination of a novel bile acid sequestrant in rodent diet by near-infrared spectroscopy

Capillary Electrochromatography as a Method Development Tool for the Liquid Chromatographic Separation of DUP 654 and Related Substances

Process and Method Variability Modeling to Achieve QbD Targets

Meeting Report: Vaccine Stability Considerations to Enable Rapid Development and Deployment

Dissolution Best Practices and International Harmonization - AAPS Workshop Report

Multifactor Non-linear Modelling for Accelerated Stability Analysis and Prediction

Multifactor non-linear modelling for accelerated stability analysis and prediction: the right approach can provide a clear, statistically defendable method for determining dissolution and accelerated stability

Strategies of Bringing Drug Product Marketing Applications to Meet Current Regulatory Standards

Method validation by design to support formulation development

Separation of diastereoisomers of DuP 105, a novel oxazolidinone antibacterial agent, by supercritical fluid chromatography on a Chiralcel OD column

Early Development GMPs for stability: an industry perspective (Part IV)

Investigation of pharmaceutical high-performance liquid chromatography assay bias using experimental design

Multifactor Non-linear Modeling for Accelerated Stability Analysis and Prediction

Degradation of a Fluoropyridinyl Drug in capsule Formulation: Degradant Identification, Proposed Degradation Mechanism, and Formulation Optimization

Microcolumn liquid chromatography of benzoyl derivatives of steroid metabolites

New biochemical separations using precolumn derivatization and microcolumn liquid chromatography

Quantitative alterations of steroid urinary profiles associated with diabetes mellitus

STEROID PROFILING STUDIES OF DIABETES MELLITUS AND THE HISTOCOMPATIBILITY-2 COMPLEX OF THE MOUSE THROUGH CHROMATOGRAPHIC METHODS (CAPILLARY GC, MICROCOLUMN LC, ANIMAL MODELS)

Early Development GMPs for Stability

Identification of out-of-trend stability results

Method validation by design to support formulation development

Multifactor non-linear modeling for accelerated stability analysis and prediction: the right approach can provide a clear, statistically defendable method for determining dissolution and accelerated stability

Identification of out-of-trend stability results, Part II

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