Post Market Surveillance for Medical Devices 2012 is a webinar that covers topics such as:
- US System
- Medical Device Reports
- Complaints (QSR)
- Corrections and Removals
- The Structure of Post Market Surveillance
- Post Production Information Collection
- Clinical Evaluation (MDD Annex X)
- Risk Management (ISO 14971)
- International Systems
- EU Vigilance
- Complaints (ISO 13485)
- Canada Adverse Event Reporting
- EU FSCA and FSN
Post Market Surveillance for Medical Devices 2012 brings together Regulatory Affairs Managers, Quality Managers, Design Control Managers and Risk Managers.
