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Developing Solid Oral Dosage Forms: Pharmaceutical Theory & Practice

Verlag: Academic Press, 2009
ISBN 10: 0444532420 / ISBN 13: 9780444532428
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Titel: Developing Solid Oral Dosage Forms: ...

Verlag: Academic Press

Erscheinungsdatum: 2009

Einband: Hardcover

Zustand: Used


This Book is in Good Condition. Clean Copy With Light Amount of Wear. 100% Guaranteed. Summary: Ch 1 Solubility of Pharmaceutical Solids Ch 2 Crystalline and Amorphous Solids Ch 3 Analytical Techniques in Solid State Characterization Ch 4 Salt Screening and Selection: New Challenges and Considerations in the Modern Pharmaceutical R&D Paradigm Ch 5 Drug Stability and Stability Studies Ch 6 Excipient Compatibility Ch 7 Theory of Diffusion and Pharmaceutical Applications Ch 8 Particle, Powder and Compact Characterization Ch 9 Polymer Properties and Characterization Ch 10 Applied Statistics in Product Development Ch 11 Oral Absorption Basics: Pathways, Physicochemical and Biological Factors, and Methods of Study Ch 12 Oral Absorption Evaluation and Prediction Ch 13 Fundamentals of Dissolution Ch 14 Dissolution Testing of Solid Products Ch 15 Bioavailability and Bioequivalence Ch 16 In Vivo Evaluation of Dosage Form Performance Ch 17 In Vitro-In Vivo Correlations: Fundamentals, Applications and Development Considerations Ch 18 Integration of physical, chemical, mechanical and biopharmaceutical properties in solid oral dosage form development Ch 19 Design and Development of Self-Emulsifying Drug Delivery Systems for Enhanced Oral Absorption of Poorly Soluble Compounds Ch 20 Rational Design of Oral Modified-Release Drug Delivery Systems Ch 21 Development of Modified-Releas Oral Dosage Forms Ch 22 Analytical Development and Validation for Solid Oral Dosage Forms Ch 23 Statistical Design and Analysis of Long Term Stabilty Studies for Drug Products Ch 24 Packaging selection for solid dosage forms Ch 25 Clincial Supplies Manufacture Ch 26 Specification Setting and Manufacturing Process Control for Solid Oral Drug Products Ch 27 Scale-Up Of Pharmaceutical Manufacturing Operation of Solid Dosage Forms Ch 28 Process Development, Optimization and Scale-Up: Powder Handling and Segregation Concerns Ch 29 Process Development and Scale-Up of Wet Granulation by High-Shear Process Ch 30 Development,Scale-Up and Optimization of Fluid-bed Granulation Ch 31 Development, Optimization and Scale-Up of Process Parameters: Roller Compaction Ch 32 Development, Optimization And Scale-Up Of Process Parameters: Compression Ch 33 Development, Optimization & Scale-Up of Process Parameters: Pan Coating Ch 34 Development, Optimization And Scale-Up Of Process Parameters: Wurster Coating Ch 35 Process Analytical Technology Ch 36 The Product Development Process Ch 37 Product Registration and Drug Approval Process Ch 38 Modern Pharmaceutical Development Regulations Ch 39 Intellectual Property in Pharmaceutical Development Ch 40 Product Life-Cycle Management. Buchnummer des Verkäufers ABE_book_usedgood_0444532420

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Inhaltsangabe: This book is intended for pharmaceutical professionals engaged in research and development of oral dosage forms. It covers essential principles of physical pharmacy, biopharmaceutics and industrial pharmacy as well as various aspects of state-of-the-art techniques and approaches in pharmaceutical sciences and technologies along with examples and/or case studies in product development. The objective of this book is to offer updated (or current) knowledge and skills required for rational oral product design and development. The specific goals are to provide readers with:

Basics of modern theories of physical pharmacy, biopharmaceutics and industrial pharmacy and their applications throughout the entire process of research and development of oral dosage forms

Tools and approaches of preformulation investigation, formulation/process design, characterization and scale-up in pharmaceutical sciences and technologies

New developments, challenges, trends, opportunities, intellectual property issues and regulations in solid product development

The first book (ever) that provides comprehensive and in-depth coverage of what's required for developing high quality pharmaceutical products to meet international standards

It covers a broad scope of topics that encompass the entire spectrum of solid dosage form development for the global market, including the most updated science and technologies, practice, applications, regulation, intellectual property protection and new development trends with case studies in every chapter

A strong team of more than 50 well-established authors/co-authors of diverse background, knowledge, skills and experience from industry, academia and regulatory agencies

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