European Pharmaceutical Review Issue 5 2019
Posted: 28 October 2019 | European Pharmaceutical Review | No comments yet
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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Issue
Related topics
Analytical techniques, Biopharmaceuticals, Bioprocessing, Distribution & Logistics, Drug Development, Drug Manufacturing, Drug Supply Chain, Excipients, Formulation, ICH guidelines, Impurities, Informatics, Ingredients, Manufacturing, QA/QC, Regulation & Legislation, Research & Development (R&D)
