Protein Characterisation (CQ3423)

Regulators expect companies to analyse their products far earlier and in far greater detail than ever before. The aim of this conference is to highlight the key technologies and issues facing analytical departments in meeting this demand and also the important role analytics plays in improving process developments. Key topics include the emergence of HX-MS and NMR in defining Higher Order Structures; Setting Critical Quality Attributes; Enabling High-Concentration Formulations; plus Stability at the Fill and Finish Stage.

Concerns over higher order structures are forcing companies to re-consider their analytical strategies and choice of instrumentation. Make sure you aren’t left behind in the race to satisfy ever demanding regulatory expectations

Professor John R. Engen, Associate Professor of Chemistry & Chemical Biology, Northeastern University, USA
Dr. Edward R. Zartler, Research Fellow, Merck, USA
Dr Fiona Greer, Director of Biochemical Services, M-Scan.Ltd, UK
Mr Antonio Datola, Researcher, Structural Characterisation, Merck Serono, Italy
Dr Rune Salbo, Researcher, Novo Nordisk, Denmark
Dr Nelly Viseux, Associate Director, Analytical Development, Shire, USA
Dr Anne Kowal, Associate Director, Millennium Pharmaceuticals, USA

Key reasons to attend Informa Life Sciences’ Protein Characterisation conference
 
·       Hear the latest on HX-MS, the new “analytical platform on the block”, and its impressive role in aiding comparability studies and defining protein conformation
·       Find out how NMR is being used to improve our knowledge of proteins – Merck’s Teddy Zartler reveals all
·      Merck Serono highlights the important role MS plays in supporting process development
·      Shire and Millennium Pharmaceuticals explain their approach to setting Critical Quality Attributes and the issues must overcome
·      Compare your protein aggregation detection methods with case studies from MedImmune and Abbott
·      Overcome issues relating to high-concentration formulations and how stability is monitored during the Fill and Finish Stage
·       Hear Synthon’s novel technique for optimising process development and Genzyme’s approach to profiling process characterisation

Recommended Workshops

Tuesday 26 October 2010

Workshop V: Product Characterisation of Biopharmaceuticals for Regulatory Requirements

WORKSHOP LEADERS
Dr Andrew Reason, Managing Director, M-Scan Ltd, UK & M-Scan GmbH, Germany
Dr Fiona Greer, Global Director, Quality Assurance, M-Scan Group.

Click Here for the full agenda

Friday 29 October 2010

Workshop Z: Practical Aspects of Protein Characterisation for Bioprocessing

WORKSHOP LEADER
Dr. Christine P. Chan, Senior Manager, Bioanalytics & Formulation, Genzyme Corporation, USA

Click Here for the full agenda
 
   
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