Don’t miss this exceptional opportunity to learn how industry teams are maintaining regulatory compliance whilst driving for greater efficiency from their regulatory systems and processes.
Six new interactive formats, including: Case Study World Café, Panel Debate, Future Think Tank, The Experience Exchange...
• Eight practical industry case studies
• 24 small, medium or large companies presenting
• 87% of attendees from industry
• Six new experience sharing areas
• Larry Callahan, Medical Informatics Staff, US Food and Drug Administration (FDA), USA (awaiting final confirmation)
• David Berglund, Senior Program Director, AstraZeneca Pharmaceuticals, UK
• Vinish Dureja, R&D IS Delivery Director, AstraZeneca, UK
• Rachel Carle, Sr. Director, Regulatory Affairs Operations, Genzyme, a Sanofi Company, US
• Jake Doran, IT Director, Global Regulatory Affairs , Janssen Research & Development, US
• Susanne Andreae, Head of Regulatory Informatics and Submission Management, EMD Serono Inc., US
• Gordon Topping, Senior Director, Submission Portfolio and Regulatory Knowledge Management (SPARK), UCB, Belgium
• Mark Morris, Associate Director, Head of Regulatory Information Systems, Eisai Limited, UK
• Gillian King, Director, Regulatory Operations, Biogen Idec, UK
• Stefan Brügger, Head of Global Document Management Berlin, Bayer Pharma AG, Germany
For more information, please visit www.informa-ls.com/CQ5226EPM.
When registering, please quote CQ5226EPM.