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Titlebook: Introduction to Quality by Design in Pharmaceutical Manufacturing and Analytical Development; Márcia Cristina Breitkreitz,Hector Goicoeche

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書目名稱Introduction to Quality by Design in Pharmaceutical Manufacturing and Analytical Development
編輯Márcia Cristina Breitkreitz,Hector Goicoechea
視頻videohttp://file.papertrans.cn/475/474092/474092.mp4
概述Covers the fundamental principles of QbD and AQbD using examples and literature reviews.Provides a detailed theory of different chemometrics methods (DOE; neural networks; multivariate calibration).Di
叢書名稱AAPS Introductions in the Pharmaceutical Sciences
圖書封面Titlebook: Introduction to Quality by Design in Pharmaceutical Manufacturing and Analytical Development;  Márcia Cristina Breitkreitz,Hector Goicoeche
描述.Written by twenty-five authors from academia, pharmaceutical industry and Pharmacopeias worldwide, this monograph covers the fundamentals and applications of Quality by Design (QbD) and Analytical Quality by Design (AQbD) in a practical and didactic manner. The book starts by describing the motivation and the urgent need for the implementation of the QbD framework in pharmaceutical development, along with the definition of its major elements: Quality Target Product Profile (QTTP), Critical Quality Attributes (CQAs), Critical Process Parameters (CPPs), Critical Material Attributes (CMAs) and the importance of using multivariate methods of Design of Experiments (DOE). The concept of life cycle and regulatory perspectives are discussed.?.Three chapters are entirely?dedicated to DOE theory from screening to optimization designs. Moreover, a comprehensive discussion on modelling and data treatment is presented. Practical aspects of QbD and DOE for pharmaceutical product and process of different dosage forms is included, as well as a practical guide of the input process variables, material attributes, intermediate, and final quality attributes for the most representative pharmaceutical
出版日期Book 2023
關鍵詞Quality by Design (QbD); Analytical Quality by Design (AQbD); Design of Experiments (DOE); Pharmaceutic
版次1
doihttps://doi.org/10.1007/978-3-031-31505-3
isbn_softcover978-3-031-31507-7
isbn_ebook978-3-031-31505-3Series ISSN 2522-834X Series E-ISSN 2522-8358
issn_series 2522-834X
copyrightAmerican Association of Pharmaceutical Scientists 2023
The information of publication is updating

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AAPS Introductions in the Pharmaceutical Scienceshttp://image.papertrans.cn/i/image/474092.jpg
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Introduction to Quality by Design in Pharmaceutical Manufacturing and Analytical Development978-3-031-31505-3Series ISSN 2522-834X Series E-ISSN 2522-8358
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Control Strategies of Solid Dosage Forms by PAT Toolsibutes (CQAs) of the processed matter. The technologies enabling these measurements are grouped under the name of “process analytical technologies” (PAT). The present chapter covers some of the most used PAT tools and the general strategy to analyze their outputs.
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Fundamentals of Design of Experiments and Optimization: Designs for Factor Screening and Data AnalysVA), whose basics are presented, together with the analysis of the validity of the results. In addition, two graphical strategies, the Pareto chart and the diagram of normal probability, are discussed. An example is used to illustrate the concepts. Suitable references are provided.
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