Medical Devices

6th & 13rd February


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


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