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9th Annual Clinical Trial Supplies & Packaging

Making the most of your clinical trial resources

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.

2011 Highlights

  • Find out about comparator study regulations from the MHRA and the effects of the Annex 13 on expiry dates
  • Hear how leading innovative companies such as UCB and Novo Nordisk develop plan their strategies
  • Listen to Boehringer Ingelheim, Merck, Novo Nordisk, Daiichi-Sankyo and Sanofi Aventis share their experiences of practical challenges around accurate and cost effective supply and management
  • Improve your practices - Discover how Boehringer manages its comparator supply
  • Mitigate your risks – Understand how to plan and achieve satisfactory IMP reconciliation within budget
  • Gain a new perspective – Hear the experiences of a clinical investigator
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Conference Sponsor

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Sponsor

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Exhibitors

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Media Partners

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Homepage speakers

Homepage speakers

Patti Seymour Senior Consultant BioProcess Technology Consultants, Inc.

Dr Marc Donath Head of the Endocrinology and Diabetes Clinic University Hospital of Basel

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


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Conference Sponsor

Conference Sponsor

Dates and Venues

11 Oct 2011 - 12 Oct 2011

Ramada Plaza Basel Conference Center

Increased Networking Opportunities: This conference is co-located with

Improving Comparator Studies

Dates to be confirmed


6th Annual

Temperature Controlled Pharmaceutical Distribution

Dates to be confirmed


Reviews

""An excellent overview in the area of clinical supplies""
AstraZeneca
""Very interesting and interactive""
Sanofi Pasteur MSD

Poll

Was your clinical trial supply chain affected by the April 2010 volcano ash cloud disruptions to the airways?

 
 

 

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