GCP and Quality in Clinical Trials 2014

Key Topics

• How effective risk-based quality management can help improve processes
• The latest updates and changing regulatory requirements
• First hand advice, updates and insight from leading industry representatives and key thought speakers including the Safety, Alliance for Clinical Research Excellence, the University of Cologne Ethics Committee and Society for Clinical Research Sites
• Practical problem solving with an interactive workshop on protocol design
• How do you define quality risk areas in risk-based monitoring
• The importance of an effective auditing strategy
• Making the move to RBM: What are the main areas of focus?
• Using RBM to assess new sites to ensure quality and GCP compliance

Who should Attend

Attendees involved in:

• Clinical Operations
• Quality Assurance
• Quality Control
• Study Operations
• Medical Quality
• Protocol Managers
• Auditors
• GCP Compliance
• Project Management
• CRA
• Quality Leads