Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence

Lingua: inglese

Editore: John Wiley & Sons Jan 2022, 2022

1119634601 / 9781119634607

Da: AHA-BUCH GmbH, Einbeck, GermaniaAHA-BUCH GmbH

Venditore con 5 stelle

Venditore AbeBooks dal 14 agosto 2006

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Condizione: Nuovo

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Spedito da Germania a U.S.A.

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Descrizione dell’articolo da parte del venditore

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.…

Codice articolo 9781119634607

Titolo
Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence
Autore
Umesh V Banakar
Editore
John Wiley & Sons Jan 2022
Anno di pubblicazione
2022
Condizione
Neu
Rilegatura
Buch
Lingua
inglese
ISBN 10
1119634601
ISBN 13
9781119634607
Peso dell'articolo
957 grammi
Dimensioni
235x157x35 mm

AHA-BUCH GmbH

Einbeck, Germania

Venditore con 5 stelle

Venditore AbeBooks dal 14 agosto 2006

Tariffe di spedizione da Germania a U.S.A.

ArticoloDa 7 a 10 giorni lavorativiDa 5 a 7 giorni lavorativi
Primo articoloEUR 35,00EUR 45,00
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