Successful Medical Device and IVD Post Market Surveillance and Vigilance Reporting 2014 is a seminar that covers topics such as:
- 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
Successful Medical Device and IVD Post Market Surveillance and Vigilance Reporting 2014 brings together medical device and IVD regulatory affairs professionals, including:
- Regulatory Affairs
- Vigilance
- Safety specialists
- International Regulatory Affairs
- Quality Assurance
- Compliance Managers
- Quality Compliance
