ISO 13485 Qualification Course – Medical Equipment – Regulatory Requirements
At the end of this course each trainee will be able to:
1. Knowledge and use all terms related to the working environment of medical equipment.
2. Awareness of the quality system associated with medical equipment.
3. Full awareness of management responsibilities related to the work of medical equipment.
4. Comprehensive awareness of the management of resources organically related to medical equipment.
5. Comprehensive knowledge of the life cycle of medical equipment.
6. Full knowledge of the analysis, measurement, and improvement system for medical equipment.