Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence (Hardcover)

Idioma: inglés

Editorial: John Wiley & Sons Inc, New York, 2022

1119634601 / 9781119634607

Librería: CitiRetail, Stevenage, Reino UnidoCitiRetail

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Vendedor de IberLibro desde 29 de junio de 2022

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Descripción del artículo del vendedor

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.…

N° de ref. del artículo 9781119634607

Título
Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence (Hardcover)
Autor
Umesh V. Banakar
Editorial
John Wiley & Sons Inc, New York
Año de publicación
2022
Estado
new
Encuadernación
Hardcover
Idioma
inglés
ISBN 10
1119634601
ISBN 13
9781119634607

CitiRetail

Stevenage, Reino Unido

Vendedor de 5 estrellas

Vendedor de IberLibro desde 29 de junio de 2022

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ArtículoDe 7 a 14 días hábilesDe 7 a 60 días hábiles
Primer artículoEUR 43,92EUR 43,92
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