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Pharmaceutical Theory & Practice
To order this title, and for more information, click here
Edited By
Yihong Qiu, Abbott Laboratories, IL, USA
Yisheng Chen, Novast Laboratories, Nantong, China
Geoff Zhang, Abbott Laboratories, IL, USA
Lirong Liu, Pfizer Inc., NJ, USA
William Porter, Abbott Laboratories, IL, USA
Description
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
Audience
PRIMARY MARKET: Pharmaceutical researchers at both pharmaceutical companies & academic institutions focused on developing solid dosage
forms fpr drug delivery.
Should investigate corporate bulk sales to heads of research at top
major pharma companies for
distribution to their R&D employees/labs.
SECONDARY MARKET: Advanced graduate level courses in the pharmaceutical sciences programs
in the US and EMEA.
113 Graduate Programs in Pharmaceutical Sciences/Technology in North America
40 Graduate Programs in Pharmaceutical
Sciences/Technology in EMEA
Contents
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
| Bibliographic details |
Hardbound, 978 pages, publication date: DEC-2008
ISBN-13: 978-0-444-53242-8
Imprint: ACADEMIC PRESS
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| Price and Ordering |
Price:
GBP 140
USD 230
EUR 155
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Last update: 31 Jan 2010
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