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  • Handbook of Modern Pharmaceutical Analysis

    Handbook of Modern Pharmaceutical Analysis by Ahuja, Satinder; Scypinski, Stephen;

    Series: Separation Science and Technology; 10;

      • GET 10% OFF

      • The discount is only available for 'Alert of Favourite Topics' newsletter recipients.
      • Publisher's listprice EUR 210.00
      • 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.

        87 097 Ft (82 950 Ft + 5% VAT)
      • Discount 10% (cc. 8 710 Ft off)
      • Discounted price 78 388 Ft (74 655 Ft + 5% VAT)

    87 097 Ft

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    Availability

    printed on demand

    Why don't you give exact delivery time?

    Delivery time is estimated on our previous experiences. We give estimations only, because we order from outside Hungary, and the delivery time mainly depends on how quickly the publisher supplies the book. Faster or slower deliveries both happen, but we do our best to supply as quickly as possible.

    Product details:

    • Edition number 2
    • Publisher Elsevier Science
    • Date of Publication 11 November 2010

    • ISBN 9780123756800
    • Binding Hardback
    • No. of pages598 pages
    • Size 246x188 mm
    • Weight 1150 g
    • Language English
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    Long description:

    Handbook of Modern Pharmaceutical Analysis, Second Edition, synthesizes the complex research and recent changes in the field, while covering the techniques and technology required for today's laboratories. The work integrates strategy, case studies, methodologies, and implications of new regulatory structures, providing complete coverage of quality assurance from the point of discovery to the point of use.

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    Table of Contents:

    Overview (Satinder Ahuja); High Throughput Screening in Drug Discovery and Development (Ken Apple); Solid-State Analysis (Harry Brittain); Degradation Studies of Drug Candidates (Karen Alsante); Analytical Considerations for Genotoxic and Other Impurities (Scott Miller); Quality by Design (James Drennen); Preformulation Studies (tba); Process Analytical Technology (Christine Richardson); Solid Dosage-Form Analysis (Joe Etse); Parenteral Dosage Form Analysis (Greg Birrer); Analysis of Alternate Drug Delivery systems (Ron Smith); Method Development for Chiral Compounds (S. Ahuja); Method Development for Early Phase Drug Development (Kevin Bynum); Method Development for Late Phase Drug Development (Ilias Jimidar); Analysis of Biomolecules (Ilias Jimidar); Setting Up Specifications (Doug Raynie); Validation of Test Methods (Jonathan Crowther); Stability Evaluations (Jessica Cha); Transferring Analytical Methods (Stephen Scypinski); Pharmaceutical Analysis Documentation (H. Chokshi); Emerging Analytical Methodologies (Jim Lander)

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