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Chemical Engineering in the Pharmaceutical Industry: Drug Product Design, Development, and Modeling

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Description:The 1st edition of Chemical Engineering in the Pharmaceutical Industry contained 44 Chapters and was 887 pages on 8 1/2 x 11 page format. The book was divided into 3 Parts: API (Active pharmaceutical ingredients), Drug Products, and Analytics. The new edition is significantly expanded and is split into two volumes, across the broad topics of Drug Substance and Drug Product, totaling 76 Chapters. Most of the original chapters are updated or expanded with additional example calculations of interest to Chemical Engineers. The API volume contains 50 chapters (22 new) while the Drug Product volume contains 26 chapters (20 new).Drug Product focuses on the development, chemical engineering and unit operations specific to the design, formulation, and manufacture of drug products. Drug product unit operations include wet and dry granulations, tableting, spray-coating, spray drying, lyophilization, hot-melt extrusion, controlled release, and direct compression for continuous processing. Technology transfer and scale-up of batch processes are exemplified experimentally and computationally. For the current professionals, in-silico process modeling tools that streamline experimental screening approaches is presented. The emerging field of continuous drug product manufacturing is also discussed. Although continuous manufacturing is in the mainstream for chemical engineers, it is unique in the pharmaceutical industry with regard to the range of scales and the complex economics associated with transforming existing batch-plant capacity to continuous processing. Basic analytics for quantitation of drug product quality attributes, such as potency, purity, content uniformity, and dissolution, are addressed with consideration of the applied statistics, process analytical technology (PAT), and process control. In addition we introduce contemporary methods of data analysis and extend these concepts into Quality by Design strategies for regulatory filings. Finally, technical chapters on commonly used software tools with examples are an important part of this book.We have made it easy for you to find a PDF Ebooks without any digging. And by having access to our ebooks online or by storing it on your computer, you have convenient answers with Chemical Engineering in the Pharmaceutical Industry: Drug Product Design, Development, and Modeling. To get started finding Chemical Engineering in the Pharmaceutical Industry: Drug Product Design, Development, and Modeling, you are right to find our website which has a comprehensive collection of manuals listed.
Our library is the biggest of these that have literally hundreds of thousands of different products represented.

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ISBN: 1119285496

Description: The 1st edition of Chemical Engineering in the Pharmaceutical Industry contained 44 Chapters and was 887 pages on 8 1/2 x 11 page format. The book was divided into 3 Parts: API (Active pharmaceutical ingredients), Drug Products, and Analytics. The new edition is significantly expanded and is split into two volumes, across the broad topics of Drug Substance and Drug Product, totaling 76 Chapters. Most of the original chapters are updated or expanded with additional example calculations of interest to Chemical Engineers. The API volume contains 50 chapters (22 new) while the Drug Product volume contains 26 chapters (20 new).Drug Product focuses on the development, chemical engineering and unit operations specific to the design, formulation, and manufacture of drug products. Drug product unit operations include wet and dry granulations, tableting, spray-coating, spray drying, lyophilization, hot-melt extrusion, controlled release, and direct compression for continuous processing. Technology transfer and scale-up of batch processes are exemplified experimentally and computationally. For the current professionals, in-silico process modeling tools that streamline experimental screening approaches is presented. The emerging field of continuous drug product manufacturing is also discussed. Although continuous manufacturing is in the mainstream for chemical engineers, it is unique in the pharmaceutical industry with regard to the range of scales and the complex economics associated with transforming existing batch-plant capacity to continuous processing. Basic analytics for quantitation of drug product quality attributes, such as potency, purity, content uniformity, and dissolution, are addressed with consideration of the applied statistics, process analytical technology (PAT), and process control. In addition we introduce contemporary methods of data analysis and extend these concepts into Quality by Design strategies for regulatory filings. Finally, technical chapters on commonly used software tools with examples are an important part of this book.We have made it easy for you to find a PDF Ebooks without any digging. And by having access to our ebooks online or by storing it on your computer, you have convenient answers with Chemical Engineering in the Pharmaceutical Industry: Drug Product Design, Development, and Modeling. To get started finding Chemical Engineering in the Pharmaceutical Industry: Drug Product Design, Development, and Modeling, you are right to find our website which has a comprehensive collection of manuals listed.
Our library is the biggest of these that have literally hundreds of thousands of different products represented.

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Chemical Engineering in the Pharmaceutical Industry: Drug Product Design, Development, and Modeling

Chemical Engineering in the Pharmaceutical Industry: Drug Product Design, Development, and Modeling

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