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European Pharmaceutical Review Issue 5 2019

Within this issue is an analysis of the impacts that low temperature can have on protein aggregation, a discussion on maintaining the safety and quality of medicines when delivered using drones and an exploration of chromatographic techniques used to identify impurities in radiopharmaceuticals. Other articles focus on regulatory non-compliance, excipients in drug formulations and ICH Q12. 

Included in this issue:

  • REGULATORY INSIGHT
    Regulatory non-compliance business interruptions
    Jenny Yu, Munich Re
  • FORMULATION, DEVELOPMENT & DELIVERY
    Beyond nutrition: vitamins and n-3 polyunsaturated fatty acids as APIs
    Eric Ciappio, DSM
  • BIOPROCESSING & BIOPRODUCTION
    Pernicious microorganisms: risks of contamination in pharma
    Marc Baiget-Francesch, Pharmaceutical Engineer and Julia Fontboté-Duran, Hospital Joan XXIII
  • MANUFACTURING, PACKAGING & LOGISTICS
    Defining the ‘New World Order’ of supply chain security
    Allan Bowyer, TraceLink
  • QA/QC & ANALYTICAL TECHNIQUES featuring: Microbiology and Chromatography
    Analytical method transfer and the supplier change processes for bacterial endotoxin testing
    Tim Sandle, Bio Products Laboratory and Kerry Skinner, Bio Products Laboratory

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