Clinical Trials in Asia 2012 (CTA 2012)

Key Topics

• Central Labs and Clinical trial supplies management in Asia
• Strategies for sourcing from Asia: Local Vs. Global CROs
• Regulatory maze & USFDA inspections in Asia
• Bio stats, Data management and Pharmacovigilance in Asia
• Strategies for successful patient recruitment and retention
• Therapeutic Area considerations for clinical studies in Asia

Who should Attend

Executives from Biotech, pharmaceutical, IT Firms, CRO’s and other solution providers with responsibilities in:

• Clinical Research Operations, Monitoring & Strategy
• Clinical Research & Development
• Clinical IT, E- Clinical systems and Compliance
• Clinical Data Management and Medical Writing
• Quality Control/Assurance/GCP
• Medical and Regulatory Affairs
• Safety Surveillance and clinical trial supplies