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. 
 - Second edition. 
 - 1 online resource 
<br/><br/>Includes bibliographical references and index. 
<br/><br/>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 
<br/><br/><label>ISBN: </label>9781119285519 1119285518 9781119600800 1119600804 9781119285502 111928550X 
<br/><br/><label>Source: </label>9781119285502  Wiley 
<br/><br/><label>LCCN: </label>2018055054 
<br/><br/><label>Nat. Bib. No.: </label>GBB930650  bnb 
<br/><br/><label>Nat. Bib. Agency Control No.: </label>019252779  Uk 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Pharmaceutical technology.<br/>Biochemical engineering.<br/>Chemical engineering.<br/>Technology, Pharmaceutical.<br/>Chemical Engineering.<br/>Drug Industry--methods.<br/>MEDICAL--Pharmacology.<br/>Biochemical engineering.<br/>Chemical engineering.<br/>Pharmaceutical technology.
<br/><br/><label>Index Terms--Genre/Form: </label><br/>Electronic books.
<br/><br/><label>LC Class. No.: </label>RS192 
<br/><br/><label>Dewey Class. No.: </label>615.1/9 
<br/><br/><label>National Library of Medicine Call No.: </label>QV 778