Modeling in the quality by design environment: Regulatory requirements and recommendations for design space and control strategy appointment.
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[1] Ingmar Nopens,et al. Uncertainty analysis as essential step in the establishment of the dynamic Design Space of primary drying during freeze-drying. , 2016, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[2] Johannes Khinast,et al. Mechanistic modeling of modular co-rotating twin-screw extruders. , 2014, International journal of pharmaceutics.
[3] Marianthi Ierapetritou,et al. Near infrared spectroscopic calibration models for real time monitoring of powder density. , 2016, International journal of pharmaceutics.
[4] Bruno C. Hancock,et al. Process modeling in the pharmaceutical industry using the discrete element method. , 2009, Journal of pharmaceutical sciences.
[5] T. De Beer,et al. Batch statistical process control of a fluid bed granulation process using in-line spatial filter velocimetry and product temperature measurements. , 2011, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[6] Gabriele Reich,et al. A quality by design study applied to an industrial pharmaceutical fluid bed granulation. , 2012, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[7] F. Podczeck,et al. Theoretical investigations into the influence of the position of a breaking line on the tensile failure of flat, round, bevel-edged tablets using finite element methodology (FEM) and its practical relevance for industrial tablet strength testing. , 2014, International journal of pharmaceutics.
[8] Roland W. Lewis,et al. A combined finite‐discrete element method for simulating pharmaceutical powder tableting , 2005 .
[9] P. Sharma,et al. Risk management and statistical multivariate analysis approach for design and optimization of satranidazole nanoparticles , 2017, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[10] Marianthi G. Ierapetritou,et al. Similarities and Differences Between the Concepts of Operability and Flexibility: The Steady-State Case , 2009 .
[11] Svetlana Ibrić,et al. Analysis of fluidized bed granulation process using conventional and novel modeling techniques. , 2011, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[12] Marianthi G. Ierapetritou,et al. Design Optimization under Parameter Uncertainty for General Black-Box Models , 2002 .
[13] Salvador García Muñoz,et al. Handling uncertainty in the establishment of a design space for the manufacture of a pharmaceutical product , 2010, Comput. Chem. Eng..
[14] C. Vora,et al. Risk based approach for design and optimization of stomach specific delivery of rifampicin. , 2013, International journal of pharmaceutics.
[15] Marianthi G. Ierapetritou,et al. Challenges and opportunities in modeling pharmaceutical manufacturing processes , 2015, Comput. Chem. Eng..
[16] Michael W. Laird,et al. Identification and prevention of antibody disulfide bond reduction during cell culture manufacturing , 2010, Biotechnology and bioengineering.
[17] Filippos Kesisoglou. The Role of Physiologically Based Oral Absorption Modelling in Formulation Development Under a Quality by Design Paradigm. , 2017, Journal of pharmaceutical sciences.
[18] Carl-Fredrik Mandenius,et al. Quality-by-design for biotechnology-related pharmaceuticals. , 2009, Biotechnology journal.
[19] K. Gernaey,et al. Good modeling practice for PAT applications: Propagation of input uncertainty and sensitivity analysis , 2009, Biotechnology progress.
[20] Johannes G Khinast,et al. An integrated Quality by Design (QbD) approach towards design space definition of a blending unit operation by Discrete Element Method (DEM) simulation. , 2011, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[21] M. Asadzadeh. An Introduction to the Finite Element Method (FEM) for Differential Equations , 2009 .
[22] J. Rantanen,et al. The Future of Pharmaceutical Manufacturing Sciences , 2015, Journal of pharmaceutical sciences.
[23] N. Shastri,et al. Design and optimization of disintegrating pellets of MCC by non-aqueous extrusion process using statistical tools. , 2016, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[24] François Bertrand,et al. Large-scale numerical investigation of solids mixing in a V-blender using the discrete element method , 2008 .
[25] Ali Hassanpour,et al. Discrete Element Method (DEM) Simulation of Powder Mixing Process , 2015 .
[26] Hervé Broly,et al. Application of the quality by design approach to the drug substance manufacturing process of an Fc fusion protein: towards a global multi-step design space. , 2012, Journal of pharmaceutical sciences.
[27] Christos Georgakis,et al. A Model-Free Methodology for the Optimization of Batch Processes: Design of Dynamic Experiments , 2009 .
[28] Satoshi Toyoshima,et al. Review Experiences and Regulatory Challenges for Pharmaceutical Development in Japan Using a Quality-by-Design Approach , 2016, Therapeutic innovation & regulatory science.
[29] Ingmar Nopens,et al. Model-based analysis of high shear wet granulation from batch to continuous processes in pharmaceutical production--a critical review. , 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[30] Hai-bin Qu,et al. In-line monitoring of alcohol precipitation by near-infrared spectroscopy in conjunction with multivariate batch modeling. , 2011, Analytica chimica acta.
[31] B. H. Ng,et al. Analysis of particle motion in a paddle mixer using Discrete Element Method (DEM) , 2011 .
[32] Pierantonio Facco,et al. Latent variable modeling to assist the implementation of Quality-by-Design paradigms in pharmaceutical development and manufacturing: a review. , 2013, International journal of pharmaceutics.
[33] Johannes G Khinast,et al. Mathematical modeling of the coating process. , 2013, International journal of pharmaceutics.
[34] René Holm,et al. Q8(R2): Pharmaceutical Development , 2017 .
[35] I. C. Sinka,et al. Analysis of tablet compaction. II. Finite element analysis of density distributions in convex tablets. , 2004, Journal of pharmaceutical sciences.
[36] Bruno C. Hancock,et al. Investigation of particle packing in model pharmaceutical powders using X-ray microtomography and discrete element method , 2006 .
[37] Davide Fissore,et al. In-Line and Off-Line Optimization of Freeze-Drying Cycles for Pharmaceutical Products , 2013 .
[38] James K. Drennen,et al. Adaptive Design Space as an Integrated Component of Quality by Design , 2012, Journal of Pharmaceutical Innovation.
[39] Rui Oliveira,et al. Hybrid modeling as a QbD/PAT tool in process development: an industrial E. coli case study , 2016, Bioprocess and Biosystems Engineering.
[40] Peter York,et al. Establishing and analyzing the design space in the development of direct compression formulations by gene expression programming. , 2012, International journal of pharmaceutics.
[41] John Strong. Chapter 27 – Scale-up of Pharmaceutical Manufacturing Operations of Solid Dosage Forms , 2009 .
[42] Fernando J. Muzzio,et al. Flowsheet models modernize pharmaceutical manufacturing design and risk assessment , 2015 .
[43] C. Kiparissides,et al. eposition and fine particle production during dynamic flow n a dry powder inhaler : A CFD approach , 2013 .
[44] Lilli Møller Andersen,et al. Quality Risk Management , 2021, Handbook of Pharmaceutical Manufacturing Formulations, Second Edition.
[45] Igor Skrjanc,et al. Tableting process optimisation with the application of fuzzy models. , 2010, International journal of pharmaceutics.
[46] Graham Cook,et al. Summary of the EMA Joint Regulators/Industry QbD workshop (London, UK; 28–29 January 2014) , 2016, PDA Journal of Pharmaceutical Science and Technology.
[47] Fernando J. Muzzio,et al. A Combined Feed-Forward/Feed-Back Control System for a QbD-Based Continuous Tablet Manufacturing Process , 2015 .
[48] Huiquan Wu,et al. Quality-by-design (QbD): an integrated multivariate approach for the component quantification in powder blends. , 2009, International journal of pharmaceutics.
[49] Ignacio E. Grossmann,et al. An index for operational flexibility in chemical process design. Part I: Formulation and theory , 1985 .
[50] Niklas Sandler,et al. Influence of raw material properties upon critical quality attributes of continuously produced granules and tablets. , 2014, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[51] J. Macgregor,et al. A Framework for the Development of Design and Control Spaces , 2008, Journal of Pharmaceutical Innovation.
[52] T. De Beer,et al. Process analytical tools for monitoring, understanding, and control of pharmaceutical fluidized bed granulation: A review. , 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[53] Ecevit Bilgili,et al. Modeling of milling processes via DEM, PBM, and microhydrodynamics , 2017 .
[54] V. D. Dimitriadis,et al. Flexibility Analysis of Dynamic Systems , 1995 .
[55] L. Peltonen. Design Space and QbD Approach for Production of Drug Nanocrystals by Wet Media Milling Techniques , 2018, Pharmaceutics.
[56] Marianthi G. Ierapetritou,et al. Modeling of Particulate Processes for the Continuous Manufacture of Solid-Based Pharmaceutical Dosage Forms , 2013 .
[57] G. Alefeld,et al. Introduction to Interval Computation , 1983 .
[58] Salvador García-Muñoz. Establishing multivariate specifications for incoming materials using data from multiple scales , 2009 .
[59] Sarfaraz K. Niazi. Pharmaceutical Quality System , 2009 .
[60] Wolter J. Fabrycky,et al. Decision evaluation with interval mathematics: a power distribution system case study , 1994 .
[61] Cyrus Agarabi,et al. Challenges and Opportunities for Biotech Quality by Design , 2015 .
[62] M. Khan,et al. Quality by design: understanding the formulation variables of a cyclosporine A self-nanoemulsified drug delivery systems by Box-Behnken design and desirability function. , 2007, International journal of pharmaceutics.
[63] T De Beer,et al. Identifying overarching excipient properties towards an in-depth understanding of process and product performance for continuous twin-screw wet granulation. , 2017, International journal of pharmaceutics.
[64] Haibin Qu,et al. Application of in-line near infrared spectroscopy and multivariate batch modeling for process monitoring in fluid bed granulation. , 2013, International journal of pharmaceutics.
[65] Michael Glodek,et al. Process Robustness - A PQRI White Paper , 2006 .
[66] Barbara Rellahan,et al. Lessons Learned from Monoclonal Antibody Applications to the Office of Biotechnology Products Quality by Design Pilot Program , 2015 .
[67] Keisuke Takagaki,et al. Numerical evaluation of the capping tendency of microcrystalline cellulose tablets during a diametrical compression test. , 2015, International journal of pharmaceutics.
[68] Marianthi G. Ierapetritou,et al. Design Space of Pharmaceutical Processes Using Data-Driven-Based Methods , 2010, Journal of Pharmaceutical Innovation.
[69] A. Gaggioli,et al. Implementing quality by design for biotech products: Are regulators on track? , 2015, mAbs.
[70] C. W. Gardiner,et al. Handbook of stochastic methods - for physics, chemistry and the natural sciences, Second Edition , 1986, Springer series in synergetics.
[71] Huolong Liu,et al. Two-compartmental population balance modeling of a pulsed spray fluidized bed granulation based on computational fluid dynamics (CFD) analysis. , 2014, International journal of pharmaceutics.
[72] Marianthi G. Ierapetritou,et al. Challenges and Opportunities in Pharmaceutical Manufacturing Modeling and Optimization , 2014 .