Study Guide

Objective

After finishing the course the student is capable of:
- Is familiar with the regulation and legislation that guide the development of medical devices
- Knows the standards that are widely used and understands their role in medical device product development
- Knows risk analysis methods and requirements
- Understands the meaning and impacts of quality systems for product development.

Content

- Legistlation and regulation of medical device development
- Product development standards
- Risk management
- Quality system
- Usability
- Software as a medical device

Evaluation scale

H-5