Product/Service
Ensuring Quality And Balancing Risks For Multiregional Clinical Trials
Source: DIA
Join industry and regulatory leaders to address multiregional clinical trial (MRCT) opportunities and risks from a global perspective.
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•Event Brochure: Ensuring Quality And Balancing Risks For Multiregional Clinical Trials
•Event Brochure: Ensuring Quality And Balancing Risks For Multiregional Clinical Trials
•Event Brochure: Ensuring Quality And Balancing Risks For Multiregional Clinical Trials
October 26-27, 2010
Bethesda, MD
Join industry and regulatory leaders to address multiregional clinical trial (MRCT) opportunities and risks from a global perspective.
Featured Topics
- Access to Medicines and Post-trial Care
- Ethical Considerations
- Intellectual Property Protection
- Understanding the Role of Human Factors, Risk Taking, and Cultural Differences in Successful MRCTs
- Statistical Methods to Determine the Consistency of Results Across Different Regions
- Regulatory Issues Across Multiple Countries When Planning a Placebo-controlled Trial
Who Should Attend
Experienced clinical research professionals seeking current knowledge of more advanced issues with the design, implementation, maintenance, analysis, and registration of multiregional clinical trials, including:
- Statisticians
- Mid- to senior-level project managers/decisionmakers
- Regulatory affairs professionals
- Medical affairs professionals
- Site directors
- Investigator site managers
- Research and strategic development professionals
- Contract research organization professionals
- Public policy and law (including intellectual property) professionals
Contact Information
Constance Burnett
Phone: 215-293-5800
Constance.Burnett@diahome.org
•Event Brochure: Ensuring Quality And Balancing Risks For Multiregional Clinical Trials
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