Developing solid oral dosage forms : pharmaceutical theory and practice /: pharmaceutical theory and practice. (2009)
- Record Type:
- Book
- Title:
- Developing solid oral dosage forms : pharmaceutical theory and practice /: pharmaceutical theory and practice. (2009)
- Main Title:
- Developing solid oral dosage forms : pharmaceutical theory and practice
- Further Information:
- Note: Edited by Yihong Qiu [and four others].
- Other Names:
- (Writer on solid dosage forms), Qiu, Yihong
- Contents:
- Ch 1Solubility of Pharmaceutical Solids; Ch 2Crystalline and Amorphous Solids; Ch 3Analytical Techniques in Solid State Characterization; Ch 4Salt Screening and Selection: New Challenges and Considerations in the Modern Pharmaceutical R&D Paradigm; Ch 5Drug Stability and Stability Studies; Ch 6Excipient Compatibility; Ch 7Theory of Diffusion and Pharmaceutical Applications; Ch 8Particle, Powder and Compact Characterization; Ch 9Polymer Properties and Characterization; Ch 10Applied Statistics in Product Development; Ch 11Oral Absorption Basics: Pathways, Physicochemical and Biological Factors, and Methods of Study; Ch 12Oral Absorption Evaluation and Prediction; Ch 13Fundamentals of Dissolution; Ch 14Dissolution Testing of Solid Products; Ch 15Bioavailability and Bioequivalence; Ch 16In Vivo Evaluation of Dosage Form Performance; Ch 17In Vitro-In Vivo Correlations: Fundamentals, Applications and Development Considerations; Ch 18Integration 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 20Rational Design of Oral Modified-Release Drug Delivery Systems; Ch 21Development of Modified-Releas Oral Dosage Forms; Ch 22Analytical Development and Validation for Solid Oral Dosage Forms; Ch 23Statistical Design and Analysis of Long Term Stabilty Studies for Drug Products; Ch 24Packaging selection forCh 1Solubility of Pharmaceutical Solids; Ch 2Crystalline and Amorphous Solids; Ch 3Analytical Techniques in Solid State Characterization; Ch 4Salt Screening and Selection: New Challenges and Considerations in the Modern Pharmaceutical R&D Paradigm; Ch 5Drug Stability and Stability Studies; Ch 6Excipient Compatibility; Ch 7Theory of Diffusion and Pharmaceutical Applications; Ch 8Particle, Powder and Compact Characterization; Ch 9Polymer Properties and Characterization; Ch 10Applied Statistics in Product Development; Ch 11Oral Absorption Basics: Pathways, Physicochemical and Biological Factors, and Methods of Study; Ch 12Oral Absorption Evaluation and Prediction; Ch 13Fundamentals of Dissolution; Ch 14Dissolution Testing of Solid Products; Ch 15Bioavailability and Bioequivalence; Ch 16In Vivo Evaluation of Dosage Form Performance; Ch 17In Vitro-In Vivo Correlations: Fundamentals, Applications and Development Considerations; Ch 18Integration 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 20Rational Design of Oral Modified-Release Drug Delivery Systems; Ch 21Development of Modified-Releas Oral Dosage Forms; Ch 22Analytical Development and Validation for Solid Oral Dosage Forms; Ch 23Statistical Design and Analysis of Long Term Stabilty Studies for Drug Products; Ch 24Packaging selection for solid dosage forms; Ch 25 Clincial Supplies Manufacture; Ch 26Specification Setting and Manufacturing Process Control for Solid Oral Drug Products; Ch 27Scale-Up Of Pharmaceutical Manufacturing Operation of Solid Dosage Forms; Ch 28 Process Development, Optimization and Scale-Up: Powder Handling and Segregation Concerns; Ch 29Process Development and Scale-Up of Wet Granulation by High-Shear Process; Ch 30Development, Scale-Up and Optimization of Fluid-bed Granulation; Ch 31Development, Optimization and Scale-Up of Process Parameters: Roller Compaction; Ch 32Development, Optimization And Scale-Up Of Process Parameters: Compression; Ch 33Development, Optimization & Scale-Up of Process Parameters: Pan Coating; Ch 34Development, Optimization And Scale-Up Of Process Parameters: Wurster Coating; Ch 35Process Analytical Technology; Ch 36 The Product Development Process; Ch 37Product Registration and Drug Approval Process; Ch 38Modern Pharmaceutical Development Regulations; Ch 39Intellectual Property in Pharmaceutical Development; Ch 40Product Life-Cycle Management … (more)
- Publisher Details:
- Place of publication not identified : Academic Press
- Publication Date:
- 2009
- Extent:
- 1 online resource (978 pages)
- Subjects:
- 615.19
Solid dosage forms
Solid dosage forms -- Research - Languages:
- English
- ISBNs:
- 9780080932729
- Related ISBNs:
- 008093272X
- Access Rights:
- Legal Deposit; Only available on premises controlled by the deposit library and to one user at any one time; The Legal Deposit Libraries (Non-Print Works) Regulations (UK).
- Access Usage:
- Restricted: Printing from this resource is governed by The Legal Deposit Libraries (Non-Print Works) Regulations (UK) and UK copyright law currently in force.
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library HMNTS - ELD.DS.30715
- Ingest File:
- 02_085.xml