Developing solid oral dosage forms :: pharmaceutical theory and practice /
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 sc...
Gespeichert in:
| Weitere Verfasser: | , , |
|---|---|
| Format: | Elektronisch E-Book |
| Sprache: | English |
| Veröffentlicht: |
Amsterdam ; Boston ; London :
Academic,
2009.
|
| Ausgabe: | 1st ed. |
| Schlagworte: | |
| Online-Zugang: | Volltext Volltext |
| Zusammenfassung: | 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. |
| Beschreibung: | 1 online resource (xxx, 943 pages) : illustrations |
| Bibliographie: | Includes bibliographical references and index. |
| ISBN: | 9780080932729 008093272X |
Internformat
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| 245 | 0 | 0 | |a Developing solid oral dosage forms : |b pharmaceutical theory and practice / |c executive editors, Yihong Qiu, Yisheng Chen, Geoff G.Z. Zhang ; associate editors, Linong Liu, William R. Porter. |
| 250 | |a 1st ed. | ||
| 260 | |a Amsterdam ; |a Boston ; |a London : |b Academic, |c 2009. | ||
| 300 | |a 1 online resource (xxx, 943 pages) : |b illustrations | ||
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| 520 | |a 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. | ||
| 504 | |a Includes bibliographical references and index. | ||
| 588 | 0 | |a Print version record. | |
| 505 | 0 | |a 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, | |
| 505 | 0 | |a 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, | |
| 505 | 0 | |a 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 | |
| 650 | 0 | |a Solid dosage forms. |0 http://id.loc.gov/authorities/subjects/sh85124623 | |
| 650 | 0 | |a Solid dosage forms |x Research. | |
| 650 | 0 | |a Drugs |x Dosage forms. |0 http://id.loc.gov/authorities/subjects/sh85039727 | |
| 650 | 0 | |a Oral medication. |0 http://id.loc.gov/authorities/subjects/sh85095244 | |
| 650 | 2 | |a Dosage Forms | |
| 650 | 2 | |a Administration, Oral | |
| 650 | 6 | |a Médicaments |x Formes pharmaceutiques solides. | |
| 650 | 6 | |a Médicaments |x Formes pharmaceutiques solides |x Recherche. | |
| 650 | 6 | |a Médicaments |x Formes pharmaceutiques. | |
| 650 | 6 | |a Médicaments |x Administration par voie orale. | |
| 650 | 7 | |a MEDICAL |x Drug Guides. |2 bisacsh | |
| 650 | 7 | |a MEDICAL |x Pharmacology. |2 bisacsh | |
| 650 | 7 | |a MEDICAL |x Pharmacy. |2 bisacsh | |
| 650 | 7 | |a MEDICAL |x Nursing |x Pharmacology. |2 bisacsh | |
| 650 | 7 | |a Oral medication |2 fast | |
| 650 | 7 | |a Drugs |x Dosage forms |2 fast | |
| 650 | 7 | |a Solid dosage forms |2 fast | |
| 650 | 7 | |a Läkemedel. |2 sao | |
| 650 | 7 | |a Läkemedelstillverkning. |2 sao | |
| 700 | 1 | |a Qiu, Yihong |c (Writer on solid dosage forms) |1 https://id.oclc.org/worldcat/entity/E39PCjCxT3HhbV4DQmg6JcKDFX |0 http://id.loc.gov/authorities/names/no2016162308 | |
| 700 | 1 | |a Chen, Yisheng. | |
| 700 | 1 | |a Zhang, Geoff G. Z. | |
| 758 | |i has work: |a Developing solid oral dosage forms (Text) |1 https://id.oclc.org/worldcat/entity/E39PCFwRJKh8PpwtCpx69Q4tXd |4 https://id.oclc.org/worldcat/ontology/hasWork | ||
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Datensatz im Suchindex
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| _version_ | 1816881689422462976 |
| adam_text | |
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| author2 | Qiu, Yihong (Writer on solid dosage forms) Chen, Yisheng Zhang, Geoff G. Z. |
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| author_GND | http://id.loc.gov/authorities/names/no2016162308 |
| author_facet | Qiu, Yihong (Writer on solid dosage forms) Chen, Yisheng Zhang, Geoff G. Z. |
| author_sort | Qiu, Yihong (Writer on solid dosage forms) |
| building | Verbundindex |
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| callnumber-sort | RS 3201 S57 D48 42009EB |
| callnumber-subject | RS - Pharmacy |
| collection | ZDB-4-EBA |
| 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 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 |
| ctrlnum | (OCoLC)316577504 |
| dewey-full | 615.19 |
| dewey-hundreds | 600 - Technology (Applied sciences) |
| dewey-ones | 615 - Pharmacology and therapeutics |
| dewey-raw | 615.19 |
| dewey-search | 615.19 |
| dewey-sort | 3615.19 |
| dewey-tens | 610 - Medicine and health |
| discipline | Medizin |
| edition | 1st ed. |
| format | Electronic eBook |
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Zhang ; associate editors, Linong Liu, William R. 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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.</subfield></datafield><datafield tag="504" ind1=" " ind2=" "><subfield code="a">Includes bibliographical references and index.</subfield></datafield><datafield tag="588" ind1="0" ind2=" "><subfield code="a">Print version record.</subfield></datafield><datafield tag="505" ind1="0" ind2=" "><subfield code="a">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,</subfield></datafield><datafield tag="505" ind1="0" ind2=" "><subfield code="a">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,</subfield></datafield><datafield tag="505" ind1="0" ind2=" "><subfield code="a">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; 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| id | ZDB-4-EBA-ocn316577504 |
| illustrated | Illustrated |
| indexdate | 2024-11-27T13:16:42Z |
| institution | BVB |
| isbn | 9780080932729 008093272X |
| language | English |
| oclc_num | 316577504 |
| open_access_boolean | |
| owner | MAIN DE-863 DE-BY-FWS |
| owner_facet | MAIN DE-863 DE-BY-FWS |
| physical | 1 online resource (xxx, 943 pages) : illustrations |
| psigel | ZDB-4-EBA |
| publishDate | 2009 |
| publishDateSearch | 2009 |
| publishDateSort | 2009 |
| publisher | Academic, |
| record_format | marc |
| spelling | Developing solid oral dosage forms : pharmaceutical theory and practice / executive editors, Yihong Qiu, Yisheng Chen, Geoff G.Z. Zhang ; associate editors, Linong Liu, William R. Porter. 1st ed. Amsterdam ; Boston ; London : Academic, 2009. 1 online resource (xxx, 943 pages) : illustrations text txt rdacontent computer c rdamedia online resource cr rdacarrier 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. Includes bibliographical references and index. Print version record. 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 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 Solid dosage forms. http://id.loc.gov/authorities/subjects/sh85124623 Solid dosage forms Research. Drugs Dosage forms. http://id.loc.gov/authorities/subjects/sh85039727 Oral medication. http://id.loc.gov/authorities/subjects/sh85095244 Dosage Forms Administration, Oral Médicaments Formes pharmaceutiques solides. Médicaments Formes pharmaceutiques solides Recherche. Médicaments Formes pharmaceutiques. Médicaments Administration par voie orale. MEDICAL Drug Guides. bisacsh MEDICAL Pharmacology. bisacsh MEDICAL Pharmacy. bisacsh MEDICAL Nursing Pharmacology. bisacsh Oral medication fast Drugs Dosage forms fast Solid dosage forms fast Läkemedel. sao Läkemedelstillverkning. sao Qiu, Yihong (Writer on solid dosage forms) https://id.oclc.org/worldcat/entity/E39PCjCxT3HhbV4DQmg6JcKDFX http://id.loc.gov/authorities/names/no2016162308 Chen, Yisheng. Zhang, Geoff G. Z. has work: Developing solid oral dosage forms (Text) https://id.oclc.org/worldcat/entity/E39PCFwRJKh8PpwtCpx69Q4tXd https://id.oclc.org/worldcat/ontology/hasWork Print version: Developing solid oral dosage forms. 1st ed. Amsterdam ; Boston ; London : Academic, 2009 9780444532428 0444532420 (OCoLC)260206308 FWS01 ZDB-4-EBA FWS_PDA_EBA https://www.sciencedirect.com/science/book/9780444532428 Volltext FWS01 ZDB-4-EBA FWS_PDA_EBA https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=249200 Volltext |
| spellingShingle | Developing solid oral dosage forms : pharmaceutical theory and practice / 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 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 Solid dosage forms. http://id.loc.gov/authorities/subjects/sh85124623 Solid dosage forms Research. Drugs Dosage forms. http://id.loc.gov/authorities/subjects/sh85039727 Oral medication. http://id.loc.gov/authorities/subjects/sh85095244 Dosage Forms Administration, Oral Médicaments Formes pharmaceutiques solides. Médicaments Formes pharmaceutiques solides Recherche. Médicaments Formes pharmaceutiques. Médicaments Administration par voie orale. MEDICAL Drug Guides. bisacsh MEDICAL Pharmacology. bisacsh MEDICAL Pharmacy. bisacsh MEDICAL Nursing Pharmacology. bisacsh Oral medication fast Drugs Dosage forms fast Solid dosage forms fast Läkemedel. sao Läkemedelstillverkning. sao |
| subject_GND | http://id.loc.gov/authorities/subjects/sh85124623 http://id.loc.gov/authorities/subjects/sh85039727 http://id.loc.gov/authorities/subjects/sh85095244 |
| title | Developing solid oral dosage forms : pharmaceutical theory and practice / |
| title_auth | Developing solid oral dosage forms : pharmaceutical theory and practice / |
| title_exact_search | Developing solid oral dosage forms : pharmaceutical theory and practice / |
| title_full | Developing solid oral dosage forms : pharmaceutical theory and practice / executive editors, Yihong Qiu, Yisheng Chen, Geoff G.Z. Zhang ; associate editors, Linong Liu, William R. Porter. |
| title_fullStr | Developing solid oral dosage forms : pharmaceutical theory and practice / executive editors, Yihong Qiu, Yisheng Chen, Geoff G.Z. Zhang ; associate editors, Linong Liu, William R. Porter. |
| title_full_unstemmed | Developing solid oral dosage forms : pharmaceutical theory and practice / executive editors, Yihong Qiu, Yisheng Chen, Geoff G.Z. Zhang ; associate editors, Linong Liu, William R. Porter. |
| title_short | Developing solid oral dosage forms : |
| title_sort | developing solid oral dosage forms pharmaceutical theory and practice |
| title_sub | pharmaceutical theory and practice / |
| topic | Solid dosage forms. http://id.loc.gov/authorities/subjects/sh85124623 Solid dosage forms Research. Drugs Dosage forms. http://id.loc.gov/authorities/subjects/sh85039727 Oral medication. http://id.loc.gov/authorities/subjects/sh85095244 Dosage Forms Administration, Oral Médicaments Formes pharmaceutiques solides. Médicaments Formes pharmaceutiques solides Recherche. Médicaments Formes pharmaceutiques. Médicaments Administration par voie orale. MEDICAL Drug Guides. bisacsh MEDICAL Pharmacology. bisacsh MEDICAL Pharmacy. bisacsh MEDICAL Nursing Pharmacology. bisacsh Oral medication fast Drugs Dosage forms fast Solid dosage forms fast Läkemedel. sao Läkemedelstillverkning. sao |
| topic_facet | Solid dosage forms. Solid dosage forms Research. Drugs Dosage forms. Oral medication. Dosage Forms Administration, Oral Médicaments Formes pharmaceutiques solides. Médicaments Formes pharmaceutiques solides Recherche. Médicaments Formes pharmaceutiques. Médicaments Administration par voie orale. MEDICAL Drug Guides. MEDICAL Pharmacology. MEDICAL Pharmacy. MEDICAL Nursing Pharmacology. Oral medication Drugs Dosage forms Solid dosage forms Läkemedel. Läkemedelstillverkning. |
| url | https://www.sciencedirect.com/science/book/9780444532428 https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=249200 |
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