Spotlight on Post Market Surveillance 2017

Topics

• FAERS – FDA Adverse Event Reporting System
• Investigating a complaint or MDR
• Best Practices
• Common Mistakes and how to avoid them
• Preparing for an FDA or NB Inspection

Who should Attend

• Individuals participating in Failure Investigations
• Complaint Specialists and Managers
• Regulatory Affairs Personnel
• Individuals analyzing Returned Products/Complaint Analysis
• Clinical Affairs Personnel
• Quality Engineers
• Compliance Specialists
• Complaint Handling Unit Personnel