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A new chapter in pharmaceutical manufacturing: 3D-printed drug products

Advanced drug delivery reviews, 2017-01, Vol.108, p.39-50

2017

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Modernizing Pharmaceutical Manufacturing: from Batch to Continuous Production

Journal of pharmaceutical innovation, 2015-09, Vol.10 (3), p.191-199

2015

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Patient-Centric Quality Standards

Journal of pharmaceutical sciences, 2024-04, Vol.113 (4), p.837-855

2024

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Re-Envisioning Pharmaceutical Manufacturing: Increasing Agility for Global Patient Access

Journal of pharmaceutical sciences, 2022-03, Vol.111 (3), p.593-607

2022

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Combining 1H NMR spectroscopy and chemometrics to identify heparin samples that may possess dermatan sulfate (DS) impurities or oversulfated chondroitin sulfate (OSCS) contaminants

Journal of pharmaceutical and biomedical analysis, 2011, Vol.54 (5), p.1020-1029

2011

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Chemometric analysis for identification of botanical raw materials for pharmaceutical use: a case study using Panax notoginseng

PloS one, 2014-01, Vol.9 (1), p.e87462-e87462

2014

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A Systematic Approach of Employing Quality by Design Principles: Risk Assessment and Design of Experiments to Demonstrate Process Understanding and Identify the Critical Process Parameters for Coating of the Ethylcellulose Pseudolatex Dispersion Using Non-Conventional Fluid Bed Process

AAPS PharmSciTech, 2017-05, Vol.18 (4), p.1135-1157

2017

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Comparing a Statistical Model and Bayesian Approach to Establish the Design Space for the Coating of Ciprofloxacin HCl Beads at Different Scales of Production

AAPS PharmSciTech, 2018-11, Vol.19 (8), p.3809-3828

2018

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Identification of heparin samples that contain impurities or contaminants by chemometric pattern recognition analysis of proton NMR spectral data

Analytical and bioanalytical chemistry, 2011-08, Vol.401 (3), p.939-955

2011

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Determination of galactosamine impurities in heparin samples by multivariate regression analysis of their (1)H NMR spectra

Analytical and bioanalytical chemistry, 2011-01, Vol.399 (2), p.635-649

2011

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Combining (1)H NMR spectroscopy and chemometrics to identify heparin samples that may possess dermatan sulfate (DS) impurities or oversulfated chondroitin sulfate (OSCS) contaminants

Journal of pharmaceutical and biomedical analysis, 2011-04, Vol.54 (5), p.1020-1029

2011

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Regulatory considerations for continuous solid oral dose pharmaceutical manufacturing

How to Design and Implement Powder-To-Tablet Continuous Manufacturing Systems, 2022

2022

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Pilot Plant Preparation of an αvβ3 Integrin Antagonist. Part 1. Process Research and Development of a (S)-β-Amino Acid Ester Intermediate: Synthesis via a Scalable, Diastereoselective Imino-Reformatsky Reaction

Organic process research & development, 2004-01, Vol.8 (1), p.51-61

2004

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Pilot-Plant Preparation of an αvβ3 Integrin Antagonist. Part 3. Process Research and Development of a Diisopropylcarbodiimide and Catalytic 1-Hydroxybenzotriazole Peptide Coupling

Organic process research & development, 2009-11, Vol.13 (6), p.1088-1093

2009

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An overview of continuous protein purification processes

Biotechnology Advances, 1990, Vol.8 (4), p.741-762

1990

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Axial dispersion in Taylor-Couette flow

AIChE journal, 1995-03, Vol.41 (3), p.723-727

1995

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A new chapter in pharmaceutical manufacturing: 3D-printed drug products

Modernizing Pharmaceutical Manufacturing: from Batch to Continuous Production

Patient-Centric Quality Standards

Re-Envisioning Pharmaceutical Manufacturing: Increasing Agility for Global Patient Access

Combining 1H NMR spectroscopy and chemometrics to identify heparin samples that may possess dermatan sulfate (DS) impurities or oversulfated chondroitin sulfate (OSCS) contaminants

Chemometric analysis for identification of botanical raw materials for pharmaceutical use: a case study using Panax notoginseng

A Systematic Approach of Employing Quality by Design Principles: Risk Assessment and Design of Experiments to Demonstrate Process Understanding and Identify the Critical Process Parameters for Coating of the Ethylcellulose Pseudolatex Dispersion Using Non-Conventional Fluid Bed Process

Comparing a Statistical Model and Bayesian Approach to Establish the Design Space for the Coating of Ciprofloxacin HCl Beads at Different Scales of Production

Identification of heparin samples that contain impurities or contaminants by chemometric pattern recognition analysis of proton NMR spectral data

Advancing Product Quality: a Summary of the Inaugural FDA/PQRI Conference

Determination of galactosamine impurities in heparin samples by multivariate regression analysis of their (1)H NMR spectra

Combining (1)H NMR spectroscopy and chemometrics to identify heparin samples that may possess dermatan sulfate (DS) impurities or oversulfated chondroitin sulfate (OSCS) contaminants

Regulatory considerations for continuous solid oral dose pharmaceutical manufacturing

Pilot Plant Preparation of an αvβ3 Integrin Antagonist. Part 1. Process Research and Development of a (S)-β-Amino Acid Ester Intermediate: Synthesis via a Scalable, Diastereoselective Imino-Reformatsky Reaction

Pilot-Plant Preparation of an αvβ3 Integrin Antagonist. Part 3. Process Research and Development of a Diisopropylcarbodiimide and Catalytic 1-Hydroxybenzotriazole Peptide Coupling

An overview of continuous protein purification processes

Axial dispersion in Taylor-Couette flow

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