Global Clinical Trials 2014

Key Topics

• Partnering with Global Investigative Sites
• How Companies are Re-Thinking Global Clinical Trials
• Regulatory Update on Global Clinical Trials and in particular Emerging Markets
• Lessons Learned from Unsuccessful Global Clinical Trials
• Risk Based Monitoring for Global Clinical Trials
• CRO Best Practices in Collaborations, Implementation and Execution of Multi-National Trials:
• Designing Patient-Centric Protocols to Increase Global Patient Engagement
• Technologies Driving Efficiencies in Global Clinical Trials
• Re-Thinking Global Patient Recruitment and the Patient Experience in Global Clinical Trials
• Reducing Protocol Complexity
• Trends of Approvals Outside the US
• Audit Inspections Update

Who should Attend

Biotech and pharmaceutical senior executives with responsibilities in:

• Clinical Research & Development
• Global Clinical Operations
• Clinical Project Management
• Clinical Outsourcing
• Clinical Strategy
• Clinical Design
• Patient Recruitment/Enrollment
• Biostatistics
• Investigators
• Medical Directors
• Protocol Design
• Ethics
• Regulatory Affairs
• Distribution

and CROs, Patient Recruitment, and Logistic and Translation companies.