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Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence: Science, Applications, and Beyond - Hardcover
- PublisherWiley
- Publication date2022
- ISBN 10 1119634601
- ISBN 13 9781119634607
- BindingHardcover
- LanguageEnglish
- Edition number1
- Number of pages560
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Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence : Science, Applications, and Beyond
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Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence - Science, Applications ,and Beyond
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Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence: Science, Applications, and Beyond
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Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence : Science, Applications, and Beyond
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Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence : Science, Applications, and Beyond
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Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence: Science, Applications, and Beyond
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Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence: Science, Applications, and Beyond
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Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence (Hardcover)
Published by
John Wiley & Sons Inc, New York, 2022
ISBN 10: 1119634601
ISBN 13: 9781119634607
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Hardcover
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Hardcover. Condition: 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. Shipping may be from multiple locations in the US or from the UK, depending on stock availability. Seller Inventory # 9781119634607
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Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence : Science, Applications, and Beyond
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Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence
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Gebunden. Condition: New. Über den AutorUmesh V. Banakar, PhD, is an independent consultant and advisor to the pharmaceutical industry and academia. He s made extensive contributions to drug product development, evaluation (both in vitro and clini. Seller Inventory # 497830423
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