Who should attend?

This event will particularly benefit professionals involved in the planning, logistics, management and implementation of e-Clinical Trials. It will introduce new e-Clinical professionals to the entire scope of their responsibilities, and upgrade the knowledge base of experienced clinical supply professionals with new technologies and processes.

From pharmaceutical, biotech and CROs:

• Clinical Project Leaders
• Heads of Clinical Operations
• Heads of Clinical Research
• Clinical Research Associates
• Clinical Trials Managers
• Clinical/Site Monitors
• Regulatory Managers
• Clinical Auditors
• Heads of Quality Control/Assurance/GCP Compliance
• Clinical Statisticians
• Programmers
• Clinical Data Managers/Co-ordinators
• Clinical IT Managers
• Clinical/Medical Advisors
• Investigators

Last year's attendees