The EU Clinical Trial Regulation MasterClass

Topics

• The best options and create successful implementation
• The new EU Clinical Trial Regulation requirements
• The new EU clinical trial authorisation process

Who should Attend

Attendees with responsibilities in:

• Clinical research
• Regulatory
• Project management
• Clinical operations
• Quality assurance (GCP auditors)
• Pharmacovigilance
• Study sites
• Vendor/CRO professionals