Medical Devices
6th & 13rd February
Topics
Review of the definition and different classifications of medical devices
Different actors and value chain of medical devices
Regulatory framework for Europe, Morocco systems
Regulation of EMA medical devices
WHO recommendations
Importance of the issue of efficiency and safety
Quality control of devices
Role of medical devices in public health issues
Marketing authorization
Marketing and certification
Traceability
Creation of a database listing incidents and clinical investigation
Market interoperability: what standards to set up and export of devices
Pricing and reimbursement of medical devices
Speakers
- Philippe Megerlin, Health Laws & Systemics
- Nabil Menasria, WHO Algieria
- Maxime Diot, Eurasanté
