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Analytical Method Development for 19 Alkyl Halides as Potential Genotoxic Impurities by Analytical Quality by Design

Molecules (Basel, Switzerland), 2022-07, Vol.27 (14), p.4437

2022

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A brief review on application of design of experiment for the analysis of pharmaceuticals using HPLC

Annales pharmaceutiques françaises, 2024-03, Vol.82 (2), p.203-228

2024

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Analytical Techniques in Pharmaceutical and Biomedical Analysis

2023

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Determination of Three Alkyl Camphorsulfonates as Potential Genotoxic Impurities Using GC-FID and GC-MS by Analytical QbD

Separations, 2022-09, Vol.9 (9), p.246

2022

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AAPS Workshop: accelerating pharmaceutical development through predictive stability approaches, April 4–5, 2016

AAPS open, 2017-09, Vol.3 (1), p.1-10, Article 8

2017

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Quality by design‐steered development and validation of analytical and bioanalytical methods for raloxifene: Application of Monte Carlo simulations and variance inflation factor

Biomedical chromatography, 2023-08, Vol.37 (8), p.e5641-n/a

2023

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Computers in Pharmaceutical Analysis

Computer Aided Pharmaceutics and Drug Delivery, 2022, p.593-621

2022

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Quality by Design for Analytical Methods

Chemical Engineering in the Pharmaceutical Industry, 2010, p.543-562

2010

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Analytical quality-by-design approach for sample treatment of BSA-containing solutions

Journal of pharmaceutical analysis, 2015-02, Vol.5 (1), p.27-32

2015

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QUALITY BY DESIGN: AN OVERVIEW OF THE BASIC CONCEPTS

Quality by Design for Biopharmaceuticals, 2011, Vol.1, p.1-8

2011

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Development of Quality-By-Design Analytical Methods

Journal of pharmaceutical sciences, 2011-03, Vol.100 (3), p.797-812

2011

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Quality by design approach for enantiomeric evaluation by RP-HPLC method of Rivaroxaban and its chiral impurity

Microchemical journal, 2023-09, Vol.192, p.108911, Article 108911

2023

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Optimization of silver nanoparticles synthesis by chemical reduction to enhance SERS quantitative performances: Early characterization using the quality by design approach

Journal of pharmaceutical and biomedical analysis, 2023-09, Vol.233, p.115475-115475, Article 115475

2023

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Quality by design approach: Regulatory need

Arabian journal of chemistry, 2017-05, Vol.10 (S2), p.S3412-S3425

2017

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‘Quality by Design’ approach for the analysis of impurities in pharmaceutical drug products and drug substances

TrAC, Trends in analytical chemistry (Regular ed.), 2018-04, Vol.101, p.24-33

2018

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The Future of Pharmaceutical Manufacturing Sciences

Journal of pharmaceutical sciences, 2015-11, Vol.104 (11), p.3612-3638

2015

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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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Lyophilization Process Design Space

Journal of pharmaceutical sciences, 2013-11, Vol.102 (11), p.3883-3887

2013

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Quality by design tool evaluated green stability-indicating UPLC content determination method for the Olanzapine and Samidorphan dosage form

Microchemical journal, 2024-02, Vol.197, p.109835, Article 109835

2024

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Quality by design based development and validation of HPLC method for simultaneous estimation of paclitaxel and vinorelbine tartrate in dual drug loaded liposomes

Microchemical journal, 2019-09, Vol.149, p.103982, Article 103982

2019

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Quality by design approach for development and validation of a RP-HPLC method for simultaneous determination of co-administered levetiracetam and pyridoxine HCl in prepared tablets

Microchemical journal, 2018-12, Vol.143, p.55-63

2018

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Forced degradation studies to assess the stability of drugs and products

TrAC, Trends in analytical chemistry (Regular ed.), 2013-09, Vol.49, p.71-88

2013

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Eco-friendly RP-HPLC UV Quantification Method for Parental Products Buffer Agents by Utilizing Polymethacrylate Resin Stationary Phase in Light of Quality by Design

Asian journal of chemistry, 2023, Vol.35 (8), p.1843-1849

2023

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QbD approach by computer aided design and response surface methodology for molecularly imprinted polymer based on magnetic halloysite nanotubes for extraction of norfloxacin from real samples

Talanta (Oxford), 2018-07, Vol.184, p.266-276

2018

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A Quality by Design (QbD) driven gradient high performance liquid chromatography method development for the simultaneous estimation of dasatinib and nilotinib in lipid nanocarriers

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2024-08, Vol.1243, p.124229, Article 124229

2024

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Analytical Method Development for 19 Alkyl Halides as Potential Genotoxic Impurities by Analytical Quality by Design

A brief review on application of design of experiment for the analysis of pharmaceuticals using HPLC

Analytical Techniques in Pharmaceutical and Biomedical Analysis

Determination of Three Alkyl Camphorsulfonates as Potential Genotoxic Impurities Using GC-FID and GC-MS by Analytical QbD

AAPS Workshop: accelerating pharmaceutical development through predictive stability approaches, April 4–5, 2016

Quality by design‐steered development and validation of analytical and bioanalytical methods for raloxifene: Application of Monte Carlo simulations and variance inflation factor

Computers in Pharmaceutical Analysis

Quality by Design for Analytical Methods

Analytical quality-by-design approach for sample treatment of BSA-containing solutions

QUALITY BY DESIGN: AN OVERVIEW OF THE BASIC CONCEPTS

Development of Quality-By-Design Analytical Methods

Quality by design approach for enantiomeric evaluation by RP-HPLC method of Rivaroxaban and its chiral impurity

Optimization of silver nanoparticles synthesis by chemical reduction to enhance SERS quantitative performances: Early characterization using the quality by design approach

Quality by design approach: Regulatory need

‘Quality by Design’ approach for the analysis of impurities in pharmaceutical drug products and drug substances

The Future of Pharmaceutical Manufacturing Sciences

Design Spaces for analytical methods

Lyophilization Process Design Space

Quality by design tool evaluated green stability-indicating UPLC content determination method for the Olanzapine and Samidorphan dosage form

Quality by design based development and validation of HPLC method for simultaneous estimation of paclitaxel and vinorelbine tartrate in dual drug loaded liposomes

Quality by design approach for development and validation of a RP-HPLC method for simultaneous determination of co-administered levetiracetam and pyridoxine HCl in prepared tablets

Forced degradation studies to assess the stability of drugs and products

Eco-friendly RP-HPLC UV Quantification Method for Parental Products Buffer Agents by Utilizing Polymethacrylate Resin Stationary Phase in Light of Quality by Design

QbD approach by computer aided design and response surface methodology for molecularly imprinted polymer based on magnetic halloysite nanotubes for extraction of norfloxacin from real samples

A Quality by Design (QbD) driven gradient high performance liquid chromatography method development for the simultaneous estimation of dasatinib and nilotinib in lipid nanocarriers

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