1, introduction of laws and regulations system of medical device management;

2, the main measures and important characteristics of medical device supervision and management;

3. Basic knowledge of medical device supervision (clinical verification);

4, adverse reactions in the process of medical device registration and technical review points;

5. Biocompatibility, tissue engineering and products;

6, passive medical device products and medical device industry status and development trend;

7, electrical safety, X-ray machine;

8, laser therapy equipment, breathing machine, ultrasonic diagnostic equipment.