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Chemical engineering in the pharmaceutical industry : drug product design, development and modeling / edited by Mary Tanya am Ende, Global R & D, Pfizer, Inc., Groton, CT, USA, David J. am Ende, Nalas Engineering Services, Inc., Centerbrook, CT, USA.

Contributor(s): Ende, Mary Tanya am [editor.] | Ende, David J. am [editor.].
Material type: materialTypeLabelBookPublisher: Hoboken, NJ, USA : Wiley, 2019Edition: Second edition.Description: 1 online resource.Content type: text Media type: computer Carrier type: online resourceISBN: 9781119285519; 1119285518; 9781119600800; 1119600804; 9781119285502; 111928550X.Subject(s): Pharmaceutical technology | Biochemical engineering | Chemical engineering | Technology, Pharmaceutical | Chemical Engineering | Drug Industry -- methods | MEDICAL -- Pharmacology | Biochemical engineering | Chemical engineering | Pharmaceutical technologyGenre/Form: Electronic books.Additional physical formats: Print version:: Chemical engineering in the pharmaceutical industry.DDC classification: 615.1/9 Online resources: Wiley Online Library
Contents:
Preface; Contributors; Unit Conversions and Commonly used Formulas; Part I Introduction; Chapter 1 Chemical Engineering in the Pharmaceutical Industry: An Introduction; Part II Drug Product Design, Development & Modeling; Chapter 2 Design of Solid Dosage Formulations; Chapter 3 Powder Process Challenges and Solutions; Chapter 4 Design and Scale-up of Dry Granulation Processes; Chapter 5 Model based development of roller compaction processes; Chapter 6 Wet Granulation Processes; Chapter 7 Towards a generic model for twin-screw wet granulation; Chapter 8 Modeling a dosator capsule filling process for hard-shell capsules; Chapter 9 Powder Compaction -- Process Design and Understanding; Chapter 10 Punch Sticking: Factors and Solutions; Chapter 11 Spray Atomization Modeling for Tablet Film Coating Processes; Chapter 12 Spray Drying and Amorphous Dispersions; Chapter 13 The Freeze Drying Process: The Use of Mathematical Modeling in Process Design, Understanding and Scale-up; Chapter 14 Sterilization Processes in the Pharmaceutical Industry; Chapter 15 Controlled Release Technology and Design of Oral Controlled Release Dosage Forms; Chapter 16 Process Design and Development for Novel Pharmaceutical Dosage Forms; Chapter 17 Multiscale Modeling of a Pharmaceutical Fluid-bed Coating Process: Using CFD/DEM and Population-balance Models to Predict Coating Uniformity; Chapter 18 Process Design of Topical Semi-solids: Application of Fundamental Concepts in Pharmaceutical Engineering to PEG Ointment Development; Chapter 19 Achieving a Hot Melt Extrusion Design Space for the Production of Solid Solutions; Chapter 20 Drug Product Process Modeling; Part III Continuous Manufacturing; Chapter 21 Continuous Manufacturing in Secondary Production; Chapter 22 Continuous Direct Compression Using Portable Continuous Miniature Modular & Manufacturing (PCM & M); Chapter 23 Process control levels for continuous pharmaceutical tablet manufacturing; Part IV Applied Statistics / Regulatory Environment; Chapter 24 Multivariate Analysis for Pharmaceutical and Medical Device Development; Chapter 25 Pharmaceutical Manufacturing: The Role of Multivariate Analysis in Design Space, Control Strategy, Process Understanding, Troubleshooting, and Optimization; Chapter 26 Quality by Design: Pilot to Reality -- The Honeymoon Phase to the Stormy Years
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Online resource; title from PDF title page (EBSCO, viewed April 8, 2019)

Includes bibliographical references and index.

Preface; Contributors; Unit Conversions and Commonly used Formulas; Part I Introduction; Chapter 1 Chemical Engineering in the Pharmaceutical Industry: An Introduction; Part II Drug Product Design, Development & Modeling; Chapter 2 Design of Solid Dosage Formulations; Chapter 3 Powder Process Challenges and Solutions; Chapter 4 Design and Scale-up of Dry Granulation Processes; Chapter 5 Model based development of roller compaction processes; Chapter 6 Wet Granulation Processes; Chapter 7 Towards a generic model for twin-screw wet granulation; Chapter 8 Modeling a dosator capsule filling process for hard-shell capsules; Chapter 9 Powder Compaction -- Process Design and Understanding; Chapter 10 Punch Sticking: Factors and Solutions; Chapter 11 Spray Atomization Modeling for Tablet Film Coating Processes; Chapter 12 Spray Drying and Amorphous Dispersions; Chapter 13 The Freeze Drying Process: The Use of Mathematical Modeling in Process Design, Understanding and Scale-up; Chapter 14 Sterilization Processes in the Pharmaceutical Industry; Chapter 15 Controlled Release Technology and Design of Oral Controlled Release Dosage Forms; Chapter 16 Process Design and Development for Novel Pharmaceutical Dosage Forms; Chapter 17 Multiscale Modeling of a Pharmaceutical Fluid-bed Coating Process: Using CFD/DEM and Population-balance Models to Predict Coating Uniformity; Chapter 18 Process Design of Topical Semi-solids: Application of Fundamental Concepts in Pharmaceutical Engineering to PEG Ointment Development; Chapter 19 Achieving a Hot Melt Extrusion Design Space for the Production of Solid Solutions; Chapter 20 Drug Product Process Modeling; Part III Continuous Manufacturing; Chapter 21 Continuous Manufacturing in Secondary Production; Chapter 22 Continuous Direct Compression Using Portable Continuous Miniature Modular & Manufacturing (PCM & M); Chapter 23 Process control levels for continuous pharmaceutical tablet manufacturing; Part IV Applied Statistics / Regulatory Environment; Chapter 24 Multivariate Analysis for Pharmaceutical and Medical Device Development; Chapter 25 Pharmaceutical Manufacturing: The Role of Multivariate Analysis in Design Space, Control Strategy, Process Understanding, Troubleshooting, and Optimization; Chapter 26 Quality by Design: Pilot to Reality -- The Honeymoon Phase to the Stormy Years

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