Clinical Trial Logistics
http://www.smi-online.co.uk/2010logistics13.asp
Following the success of the last few years, this year's conference will provide you with the tools necessary to manage your supply chain effectively and ensure that your trials finish on time and within budget.
Our expert line-up of speakers includes:
- Didier Basseras, Senior Director, Global Clinical Packaging Operations, Clinical Supply Chain, Sanofi-Aventis
- Dawn Padfield, Director of Technical Development and Clinical Supply, Norgine
- Frederico Lupp, Director Sales Europe and Latin America, LifeConEx
- Tim Saint, Business Development Manager, Marken
- Mark Wright, Validation Consultant, GxP Consulting
- Robert Silber, Director, Supply Chain Management, FibroGen
- Heike Roeder, Director, Global Head of Clinical Trial Supply Planning, UCB
- Paul Ranson, Partner, Fasken Martineau LLP
- Geert Crauwels, Director, Lodestone
Plus, why not attend our interactive post-conference workshops?
Do you really know what happens to your IMPs at the clinical trial site?
19th May 2010, London Marriott Hotel Regents Park, London.
This will be lead by Rita Hattemer-Apostel, CEO, Verdandi AG.
Designing the clinical supply chain – techniques, concepts, partners and geographical differences
Techniques, concepts, partners and geographical differences
19th May 2010, London Marriott Hotel Regents Park, London.
This will be lead by Johan Beukema, Partner, Buck Consultants International.




