Risk Management Plan Summit 2017

Topics

• App/technological tool as a medium to monitor and track activities at the local level
• Regulations globally including EMA’s GVP Modules V and XVI
• Tailor communications to the needs of specific patients with disparate backgrounds
• Implement and harmonise on a global scale from a regional or centralised model with cross-functional teams
• Drug safety and patient outcomes and incorporate analysis into modifications

Who should Attend

Attendees from pharmaceutical and biotechnology companies responsibile for:

• Epidemiology/Pharmacoepidemiology
• Benefit/Risk Management
• Biostatistics
• Global/Regional Pharmacovigilance
• Risk Analysis/Assessment
• Medical Writing
• Local/Regional Medical Safety
• Global Drug/Product Safety
• Medical Information
• Safety Evaluation/Reporting
• Therapy Area Safety
• Patient Safety
• Safety Surveillance/Operations
• Integrated Medical Safety
• Clinical Risk Management
• Clinical Data Management
• Compliance Management
• Regulatory Affairs/Legal
• Pre/Post Marketing
• Patient Engagement
• Life Cycle Management