Stability Challenges III: Assuring the stability of medicines from manufacture to use

12 October 2017 10:00-16:30, London, United Kingdom

Continuing our successful Stability Challenges series, this is an essential event for anyone concerned with the management and assessment of drug stability:
• Hear from individuals involved in the regulation and inspection of stability and GDP
• Learn from industry experts on scientific developments in stability study design and interpretation
• Debate practical issues for clinical trials and amorphous drug formulations
• Examine ways to improve compliance and productivity in stability testing
• Network with other professionals and exhibitors

You will leave this event with:
• Best practice and case studies from regulatory and industry experts
• Understanding of key developments, issues and strategies in drug stability
• Improve your stability laboratory compliance and efficiency
• New connections to experts and opinion leaders in this field
• Assure the stability of your medicines
  • Nigel McSweeney, Cuspor, Ireland
  • Dr Niels Hartvig Novo Nordisk, United Kingdom
  • Liselotte Kamper Novo Nordisk, United Kingdom
  • Dr Garry Scrivens, Pfizer, United Kingdom
  • Dr Samuel Kyeremateng NCE Formulation Sciences, AbbVie Deutschland GmbH, Germany
  • Dr Kristin Lehmkemper, NCE Formulation Sciences, AbbVie Deutschland GmbH, Germany

Sponsorship & supporting organisations
Royal Pharmaceutical Society and Royal Society of Chemistry
The Royal Society of Chemistry

The Royal Society of Chemistry, Burlington House, Piccadilly, London, W1J 0BA, United Kingdom

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