banakar umesh (30 resultados)

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Hardback. Condición: New. Explore the cutting-edge of dissolution testing in an authoritative, one-stop resource In Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence: Science, Applications, and Beyond, distinguished pharmaceutical advisor and consultant Dr. Umesh Banakar delivers a comprehensive and up-to-date reference covering the established and emerging roles of dissolution testing in pharmaceutical drug development. After discussing the fundamentals of the subject, the included resources go on to explore common testing practices and methods, along with their associated challenges and issues, in the drug development life cycle. Over 19 chapters and 1100 references allow practicing scientists to fully understand the role of dissolution, apart from mere quality control. Readers will discover a wide range of topics, including automation, generic and biosimilar drug development, patents, and clinical safety. This volume offers a one-stop resource for information otherwise scattered amongst several different regulatory regimes. It also includes: A thorough introduction to the fundamentals and essential applications of pharmaceutical dissolution testingComprehensive explorations of the foundations and drug development applications of bioavailability and bioequivalencePractical discussions about solubility, dissolution, permeability, and classification systems in drug developmentIn-depth examinations of the mechanics of dissolution, including mathematical models and simulationsAn elaborate assessment of biophysiologically relevant dissolution testing and IVIVCs, and their unique applicationsA complete understanding of the methods, requirements, and global regulatory expectations pertaining to dissolution testing of generic drug products Ideal for drug product development and formulation scientists, quality control and assurance professionals, and regulators, Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence is also the perfect resource for intellectual property assessors.

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Hardcover. Condición: Brand New. 500 pages. 9.29x6.34x1.34 inches. In Stock.

Hardback. Condición: New. Explore the cutting-edge of dissolution testing in an authoritative, one-stop resource In Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence: Science, Applications, and Beyond, distinguished pharmaceutical advisor and consultant Dr. Umesh Banakar delivers a comprehensive and up-to-date reference covering the established and emerging roles of dissolution testing in pharmaceutical drug development. After discussing the fundamentals of the subject, the included resources go on to explore common testing practices and methods, along with their associated challenges and issues, in the drug development life cycle. Over 19 chapters and 1100 references allow practicing scientists to fully understand the role of dissolution, apart from mere quality control. Readers will discover a wide range of topics, including automation, generic and biosimilar drug development, patents, and clinical safety. This volume offers a one-stop resource for information otherwise scattered amongst several different regulatory regimes. It also includes: A thorough introduction to the fundamentals and essential applications of pharmaceutical dissolution testingComprehensive explorations of the foundations and drug development applications of bioavailability and bioequivalencePractical discussions about solubility, dissolution, permeability, and classification systems in drug developmentIn-depth examinations of the mechanics of dissolution, including mathematical models and simulationsAn elaborate assessment of biophysiologically relevant dissolution testing and IVIVCs, and their unique applicationsA complete understanding of the methods, requirements, and global regulatory expectations pertaining to dissolution testing of generic drug products Ideal for drug product development and formulation scientists, quality control and assurance professionals, and regulators, Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence is also the perfect resource for intellectual property assessors.

Condición: New. 2022. 1st Edition. Hardcover. . . . . . Books ship from the US and Ireland.

Gebunden. Condición: New. Introduction, Historical Highlights, and the Need for Dissolution Testing Theories of Dissolution Dissolution Testing Devices Automation in Dissolution Testing, by William A. Hanson and Albertha M. Paul Factors That Influence Dissolution Testing Interpretat.

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Buch. Condición: Neu. Neuware - Explore the cutting-edge of dissolution testing in an authoritative, one-stop resource In Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence: Science, Applications, and Beyond, distinguished pharmaceutical advisor and consultant Dr. Umesh Banakar delivers a comprehensive and up-to-date reference covering the established and emerging roles of dissolution testing in pharmaceutical drug development. After discussing the fundamentals of the subject, the included resources go on to explore common testing practices and methods, along with their associated challenges and issues, in the drug development life cycle. Over 19 chapters and 1100 references allow practicing scientists to fully understand the role of dissolution, apart from mere quality control. Readers will discover a wide range of topics, including automation, generic and biosimilar drug development, patents, and clinical safety. This volume offers a one-stop resource for information otherwise scattered amongst several different regulatory regimes. It also includes: - A thorough introduction to the fundamentals and essential applications of pharmaceutical dissolution testing - Comprehensive explorations of the foundations and drug development applications of bioavailability and bioequivalence - Practical discussions about solubility, dissolution, permeability, and classification systems in drug development - In-depth examinations of the mechanics of dissolution, including mathematical models and simulations - An elaborate assessment of biophysiologically relevant dissolution testing and IVIVCs, and their unique applications - A complete understanding of the methods, requirements, and global regulatory expectations pertaining to dissolution testing of generic drug products Ideal for drug product development and formulation scientists, quality control and assurance professionals, and regulators, Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence is also the perfect resource for intellectual property assessors.

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Buch. Condición: Neu. Neuware.

Hardcover. Condición: New. HardCover. Pub Date: 2023-10 Pages: 343 Language: Chinese Publisher: Chemical Industry Press Drug Dissolution Test. Bioavailability and Bioequivalence: Science. Application and Future has 19 chapters in total. The main contents include: Drugs Basic principles and practical applications of dissolution and dissolution; drug dissolution test methods; content related to bioavailability and bioequivalence; dissolution data analysis and in vitro and in vivo correlation. etc. Drug Dissolution Testin.

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Hardcover. Condición: new. Hardcover. Explore the cutting-edge of dissolution testing in an authoritative, one-stop resource In Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence: Science, Applications, and Beyond, distinguished pharmaceutical advisor and consultant Dr. Umesh Banakar delivers a comprehensive and up-to-date reference covering the established and emerging roles of dissolution testing in pharmaceutical drug development. After discussing the fundamentals of the subject, the included resources go on to explore common testing practices and methods, along with their associated challenges and issues, in the drug development life cycle. Over 19 chapters and 1100 references allow practicing scientists to fully understand the role of dissolution, apart from mere quality control. Readers will discover a wide range of topics, including automation, generic and biosimilar drug development, patents, and clinical safety. This volume offers a one-stop resource for information otherwise scattered amongst several different regulatory regimes. It also includes: A thorough introduction to the fundamentals and essential applications of pharmaceutical dissolution testingComprehensive explorations of the foundations and drug development applications of bioavailability and bioequivalencePractical discussions about solubility, dissolution, permeability, and classification systems in drug developmentIn-depth examinations of the mechanics of dissolution, including mathematical models and simulationsAn elaborate assessment of biophysiologically relevant dissolution testing and IVIVCs, and their unique applicationsA complete understanding of the methods, requirements, and global regulatory expectations pertaining to dissolution testing of generic drug products Ideal for drug product development and formulation scientists, quality control and assurance professionals, and regulators, Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence is also the perfect resource for intellectual property assessors. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.

Hardcover. Condición: Brand New. 500 pages. 9.29x6.34x1.34 inches. In Stock. This item is printed on demand.