This years agenda will provide you with all the latest strategies to implement into your global clinical trial supply processes that will allow you to improve the forecasting, resource planning, labelling, packaging and distribution of drugs to increase the efficiency of your global clinical trials. This is a must for anyone who is involved in the clinical supply chain and also for ensuring that all regulations around this are met.
This year’s event will address the specific challenges of delivering timely, compliant IMP and supplies within budget. There will also be sessions devoted to the latest trends and technologies in forecasting, adaptive clinical trials, comparator products and the issues surroundings providing supplies to new and emerging economies.
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Peter Feldschreiber, Barrister Four New Square, Lincolns Inn London and Senior Medical Assessor, MHRA
Dr Marc Donath, Head of the Endocrinology and Diabetes Clinic, University Hospital of Basel
Ewald Kamp, Project lead ECS - CLARA: Excellence in Clinical Supply, Global Investigational Product Supply (Dept. PTDS), F. Hoffmann-La Roche AG
Peter Orosz, Head of Clinical Supply Chain Management, Oncology, Boehringer Ingelheim
Didier Basseras, SCP - Clinical Supplies Vice President, Sanofi Aventis
Frauke Bruns, Clinical Trial Supplies Group Leader, Actelion Pharmaceuticals Ltd.
Karen Heede Crosbie, Clinical Supplies Coordination, Novo Nordisk A/S
Heike Roeder, Director Head Global Training, SOP and Process improvement, UCB
David Gilliland, Director, Clinical Supply Operations Pharmaceutical Development, Daiichi Sankyo Pharma Development
Sue Lee, Regional Quality Manager – UKIMEA UK, Ireland, Middle East & Africa, World Courier Logistics Ltd.
Martina Müller, Outsourcing Manager, Boehringer Ingelheim
Birgit Molander, Global Business Coordinator, Modified Comparators, Sanofi Aventis
""An excellent overview in the area of clinical supplies""
""Very interesting and interactive""