Successful Medical Device and IVD Post Market Surveillance and Vigilance Reporting 2014

Key Topics

• Gain a clear understanding of your responsibilities as a manufacturer
• Build successful Post Market Surveillance strategies
• Ensure you know what vigilance data you should be reporting
• Manage risk effectively to avoid product recall
• Understand all interpretations of the Medical Device Directive for successful PMS across the EU
• Update on the latest reporting strategies for vigilance data
• Get critical updates on PMS requirements from outside of the EU

Who should Attend

Medical device and IVD regulatory affairs professionals, including:

• Regulatory Affairs
• Vigilance
• Safety specialists
• International Regulatory Affairs
• Quality Assurance
• Compliance Managers
• Quality Compliance