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    Pharmaceutical Quality by Design: Principles and Applications

    Pharmaceutical Quality by Design by Beg, Sarwar; Hasnain, Md Saquib;

    Principles and Applications

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      • Publisher's listprice EUR 175.00
      • The price is estimated because at the time of ordering we do not know what conversion rates will apply to HUF / product currency when the book arrives. In case HUF is weaker, the price increases slightly, in case HUF is stronger, the price goes lower slightly.

        74 235 Ft (70 700 Ft + 5% VAT)
      • Discount 10% (cc. 7 424 Ft off)
      • Discounted price 66 812 Ft (63 630 Ft + 5% VAT)

    74 235 Ft

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    Product details:

    • Publisher Academic Press
    • Date of Publication 29 March 2019

    • ISBN 9780128157992
    • Binding Paperback
    • No. of pages448 pages
    • Size 228x152 mm
    • Weight 700 g
    • Language English
    • 7

    Categories

    Long description:

    Pharmaceutical Quality by Design: Principles and Applications discusses the Quality by Design (QbD) concept implemented by regulatory agencies to ensure the development of a consistent and high-quality pharmaceutical product that safely provides the maximum therapeutic benefit to patients. The book walks readers through the QbD framework by covering the fundamental principles of QbD, the current regulatory requirements, and the applications of QbD at various stages of pharmaceutical product development, including drug substance and excipient development, analytical development, formulation development, dissolution testing, manufacturing, stability studies, bioequivalence testing, risk and assessment, and clinical trials.

    Contributions from global leaders in QbD provide specific insight in its application in a diversity of pharmaceutical products, including nanopharmaceuticals, biopharmaceuticals, and vaccines. The inclusion of illustrations, practical examples, and case studies makes this book a useful reference guide to pharmaceutical scientists and researchers who are engaged in the formulation of various delivery systems and the analysis of pharmaceutical product development and drug manufacturing process.

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    Table of Contents:

    1. Introduction to Quality by Design (QbD): Fundamentals, principles
    2. Global regulatory perspectives on Quality by Design in pharma manufacturing
    3. Application of Design of Experiments (DoE) in pharmaceutical product and process optimization
    4. QbD considerations for excipient manufacturing
    5. QbD considerations for analytical development
    6. Application of Quality by Design paradigms for development of solid dosage forms
    7. QbD considerations for topical and transdermal product development
    8. Qbd based development of pharmaceutical parenteral drug products: An overview
    9. Quality by design considerations for product development of dry-powder inhalers
    10. QbD considerations for development of lyophilized products
    11. Application of quality by design approach for hot-melt extrusion process optimization
    12. QbD applications for development of nanopharmaceutical products
    13. Application of QbD principles in nanocarrier based drug delivery systems
    14. Application of QbD framework for development of self-emulsifying drug delivery systems
    15. 'Quality by Design' approach for development of multiparticulate drug delivery systems
    16. Application of QbD elements for development of vesicular drug delivery systems
    17. Emergence of quality by design in extraction technology for bioactive compounds
    18. Application of quality by design for the development of biopharmaceuticals

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