Why should I attend?

Last year there was an excessive increase in the number of high-profile recalls or safety warnings that impacted the pharmaceutical and medical device industries, resulting in the immediate assembly of task forces and attention by the FDA. As a result, the FDA is placing an increasing priority on companies to assume the responsibility of increasing transparency of clinical trial data, as well as ensuring full disclosure of findings post-market.

Implementation of strategies for clinical data transparency and disclosure within an evolving regulatory framework are imperative for pharma companies to successfully execute clinical trials and ensure the appropriate information is conveyed to the FDA and, ultimately to the patient.

IQPC’s Clinical Trials Supply Chain Management Conference provides information on best practices and solutions for the most complex challenges in the supply and distribution of clinical trial materials.

We Promise to Deliver the Following:

• 20+ Industry Leaders with Expert Presentation
• 3 Interactive Workshops
• 4+ Hours of Scheduled Networking Opportunities
• Open Q&A Time After Each Presentation

Who will I meet and who is speaking?

With industry experts, including:

• KEYNOTE: Dr. Jan Lewis Brandes, M.D. Assistant Clinical Professor, Neurology, Nashville Neuroscience Group
• Eric Eisenstein, DBA, Assistant Professor in Medicine, Duke Clinical Research Institute
• Collette Houston, Director, Office of Clinical Research, Memorial Sloan-Kettering Cancer Center
• Doug Meyer, Senior Director, Aptuit Informatics
• David Glynn, Drug Supply Management, Novartis Pharmaceuticals Corporation
• Mike Cohen, Director of Business Development, Myoderm Medical
• Catherine Hall, Supply Chain Management, Pfizer
• Michael Colacino, Associate Director, Clinical Manufacturing, Genyzyme Drug & Biomaterial R&D
• Adam Fleischacker, PhD Candidate, Department of Management Science and Information System, Rutgers Business School
• RS Kumar, Senior Manager, Life Sciences, BearingPoint

VPs/ Directors/ Managers from Pharmaceutical and Biotech, Consultants, and Service Providers involved in the following:

• Clinical/Investigational Supply
• Clinical Development
• Clinical Trial Operations
• Clinical Trial Supply
• Clinical Trial Logistics
• Clinical Trial Production Managers
• Clinical Research Associates
• Shipping and Distribution
• Clinical Research/Planning
• Clinical Supplies Manufacturing
• Drug Supply Management
• Purchasing
• Packaging/Labeling
• Formulation Development Scientists involved in CTM product development
• QA/QC Professionals
• Regulatory Professionals

Topics that will be addressed:

• Risk based CTM production
• Cold chain clinical supplies
• On-demand packaging and labeling
• Demand forecasting and supply/re-supply
• Clinical manufacturing processes
• Managing variations and responses to change

If you are not yet ready to register, feel free to request a reminder nearer the time .

Conference Partners

Sponsor	Media Partners

[ Register Now] · [ Next: Conference Day One: Tuesday, June 24, 2008 ]