Who should attend?

The audience will be primarily comprised of European pharma,
generics and biotech manufacturers from the following disciplines:

• Pharmacovigilance
• Medical Affairs/Medical Director/Medical Advice/Information
• QP/Deputy QP for Pharmacovigilance
• Drug Safety/Clinical Safety
• Clinical Risk Management/Compliance
• Regulatory Affairs
• Product Safety and Quality Management
• Epidemiology
• Clinical Development/Operations

Job Titles of previous attendees to Pharmacovigilance and Risk Management