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Issue #5 2015 – Digital edition

22 October 2015  •  Author(s): European Pharmaceutical Review

In the digital version of Issue #5 2015:

  • European Pharmaceutical Review Issue #5 2015FOREWORD: The importance of good distribution practice
    David Elder, GlaxoSmithKline and JPAG
  • COUNTERFEIT DRUGS: Counterfeit medicines and the need for a global approach
    David Shore, Pfizer
  • REGULATORY INSIGHT: New third-party audit scheme for excipient suppliers
    Iain Moore, President, EXCiPACT asbl
  • IN-DEPTH FOCUS: RAMAN
    Featuring articles from Sulaf Assi, Bournemouth University, Sulayman A. Oladepo, Hui Wang, David Barona and Reinhard Vehring, University of Alberta
  • PAT SERIES: Continuous manufacturing in pharma – an unstoppable trend?
    Bernhard Gutmann and Christian Oliver Kappe, University of Graz
  • POLYMORPHS: Promiscuous multicomponent drug crystals
    Masataka Ito, Kiyohiko Sugano and Katsuhide Terada, Faculty of Pharmaceutical Sciences, Toho University
  • IN-DEPTH FOCUS: RMM
    Featuring articles from David Roesti and Erik Wilkens, Novartis, Mostafa Eissa, Hikma Pharmaceuticals, and Hideharu Shintani, Chuo University
  • PARTICLE SIZING: Meeting biopharmaceutical analytical requirements for subvisible particle sizing and counting
    John Carpenter, University of Colorado, Amber Haynes Fradkin, KBI Biopharma, and Christina Vessely, Biologics Consulting Group Inc.
  • FREEZE DRYING: Dynamic vapour sorption of freeze-dried pharmaceuticals
    Claudia Kunz & Henning Gieseler, University of Erlangen

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