European Pharmaceutical Review Issue 2 2020
Posted: 21 April 2020 | European Pharmaceutical Review | No comments yet
This issue focuses on the regulatory challenges associated with increased ventilator demand during COVID-19, as well as articles investigating the use of LC-MS for protein characterisation, improving efficiency with continuous processing and the risks posed by cleanroom contaminants. Other features discuss the continual evolution of solid dosage forms and the opportunities that biosimilars present for pharma.
Included in this issue:
- COVID-19
COVID-19: the great ventilator challenge
Adrian Toutoungi, Taylor Wessing - REGULATORY INSIGHT
Tax competition in Life Sciences – how does the UK shape up?
Lawrence Wild and Richard Turner, FTI Consulting - FORMULATION, DEVELOPMENT & DELIVERY
Nanoparticle delivery offers a possible alternative to opioid pain relief
Nigel Bunnett, New York University - BIOPROCESSING & BIOPRODUCTION
Application of liquid chromatography in characterisation of lipid nanoparticle-based
oligonucleotides
Adam Socia, Yuejie Zhao and Yong Liu, MSD - QA/QC & ANALYTICAL TECHNIQUES with a special focus on Chromatography & Microbiology
How modern chromatography data systems are improving regulatory compliance in pharmaceutical manufacturing
Theresa Webster, Broughton Laboratories and Dr Kyle D’Silva, Thermo Fisher Scientific - MANUFACTURING, PACKAGING & LOGISTICS
Latest innovations in child-resistant pharmaceutical packaging
Rich Quelch, Origin
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Issue
Related topics
Analytical techniques, Biopharmaceuticals, Bioprocessing, Drug Delivery Systems, Drug Development, Drug Manufacturing, Liquid Chromatography - Mass Spectrometry (LC-MS), Manufacturing, Packaging, Production, Proteins, QA/QC, Regulation & Legislation, Research & Development (R&D), Therapeutics
