- email:registrations@informa-ls.com
- phone:+44(0)20 7017 7481
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Impurities 2011
14 - 15 September 2011
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Impurities 2011
Optimising the effectiveness of your detection, identification and control strategies for impurities
Key Themes:
- Essential regulatory updates
- Synthesising the API: managing impurities
- Detecting, identifying and quantifying impurities
- Manufacturing the finished product: managing impurities
- Controlling impurities
The programme for this conference is currently being put together, if you would be interested in participating or would like more information please contact rachael.mulcaster@informa.com
2011 Conference Highlights
Speaker Panel
Speaker Panel
Piet Christiaens
Scientific Director
Toxikon Europe, Belgium
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Rolf Schulte Oestrich
Head of Analytical Development
F. Hoffmann-La Roche AG, Switzerland
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Karen Alsante
Research Fellow
Pfizer, USA
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Mark Argentine
Senior Research Advisor, Analytical Sciences R&D
Eli Lilly, USA
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Philippe Lienard
Head of Early Development Unit
Sanofi-Aventis, France
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Xavier Molins
Head of R&D and Regulatory Affairs (EU)
Bimeda Ireland
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Rui Cerdeira
Head of QC
Bial Portela Ca SA, Portugal
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Brian Pack
Research Advisor
Eli Lilly, USA
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- Simeon Gill, Pharmaceutical Assessor, MHRA, UK
- Antonio Giordani, Director, R&D Chemistry Drug Development & OS, Rottapharm, Italy
- Simon Hamilton, Research Fellow, Merck, UK
- Thomas Anderson, Associate Principal Scientist, AstraZeneca, Sweden
- Jesper Larsen, Specialist, Quality SOE, Lundbeck, Denmark
Who should attend?
Heads of Department, Directors, Managers, Associates, Specialists and Coordinators from:
- Analytical chemistry
- Structural chemistry
- Analytical Validation
- Pharmaceutical Development
- Toxicology
- Stability Testing
- QA/QC
- Technical Affairs
- Pre-clinical Safety
- Safety Pharmacology
- Analytical R&D
Additional Workshops
Great Networking!
Don’t miss this opportunity to discuss challenges, solutions and new opportunities with fellow colleagues from industry
Promotional Opportunities!
For information on our wide-range of tailored sponsorship solutions, please contact: Chamatkar Sandhu, Email: chamatkar.sandhu@informa.com
Spotlight Session Sponsor
Media Partners
Dates and Venues
14 Sep 2011 - 15 Sep 2011
Angelo Hotel Prague
Spotlight Session Sponsor
New Speaker!
Extractable & Leachable Testing for Pharmaceutical Container/Closure Systems
Designing the Right Testing Strategy for Identification and Quantification
- Introduction: Definitions and Regulatory Requirements
- Analytical Methods required for Extractables & Leachables Research
- The TOX-RAY Screener Database, assisting in the unique identification of >2000 Extractables
- GC-ToF and LC-Accurate Mass Measurements: necessary tools in the further Identification of Unkown Compounds
- Confirmation of the identity of Extractables and Leachables through Organic Synthesis
- Case Studies
Dr. Piet Christiaens, Scientific Director, Toxikon Europe, Belgium
www.toxikon.be
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