• GDPR in Pharmacovigilance: Impact and Management of Data
• Signalling and emerging safety issues
• Inspections: Hot Topics
• Safety Agreements
• EV Requirements: Where are we now?
• Implementation of EU Clinical Trial Regulation
• Risk Management Plan

Established professionals who are seeking to increase their network of like-minded colleagues; share their thoughts and practices with others; learn the most current regulatory views and gain practical knowledge in key areas in pharmacovigilance, including:

• Signal management
• Data Privacy
• Risk Management Planning
• PSMF maintenance
• Clinical Trials

Professionals involved in:

• Drug Safety/Pharmacovigilance
• Risk Management, including Risk Evaluation and Mitigation Strategies (REMS)
• Benefit-risk assessment and communication
• Medical Product Safety Assessment
• Regulatory Affairs
• Clinical Trials
• Pharmaceuticals, biologics, combination products, devices
• Clinical Research and Clinical Research Organizations
• Health Outcomes
• Academic Research Centers
• Regulatory Agencies 

• Seek direct answers to the business challenges you are facing every day
• Understand how other organisations are managing through the shift of sharing all information to sharing relevant information
• Ensure that your pharmacovigilance work matches up with inspector expectations, and delivers efficient outcomes for patients.