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Pharmaceutical Dissolution Testing Bioavailability And Bioequivalence Science Applications And Beyond Umesh V Banakar

  • SKU: BELL-46246852
Pharmaceutical Dissolution Testing Bioavailability And Bioequivalence Science Applications And Beyond Umesh V Banakar
$ 31.00 $ 45.00 (-31%)

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Pharmaceutical Dissolution Testing Bioavailability And Bioequivalence Science Applications And Beyond Umesh V Banakar instant download after payment.

Publisher: Wiley
File Extension: PDF
File size: 10.92 MB
Pages: 560
Author: Umesh V. Banakar
ISBN: 9781119634607, 1119634601
Language: English
Year: 2022

Product desciption

Pharmaceutical Dissolution Testing Bioavailability And Bioequivalence Science Applications And Beyond Umesh V Banakar by Umesh V. Banakar 9781119634607, 1119634601 instant download after payment.

Explore the cutting-edge of dissolution testing in an authoritative, one-stop resource

InPharmaceutical 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 Bioequivalenceis also the perfect resource for intellectual property assessors.

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