1. Responsible for establishing and implementing the quality management system, and reporting the operation and improvement needs of the quality management system to the person in charge of the production enterprise;

2. Organize the internal medical device production quality management training in the production enterprise, and improve the employees' awareness and ability to comply with relevant laws and regulations and meet customer requirements;

3. Organize the collection of product quality information, and promptly report the defects of the quality management system to the person in charge of the production enterprise, as well as product complaints, adverse event monitoring and product safety hazards;

1. Responsible for establishing and implementing the quality management system, and reporting the operation and improvement needs of the quality management system to the person in charge of the production enterprise;

2. Organize the internal medical device production quality management training in the production enterprise, and improve the employees' awareness and ability to comply with relevant laws and regulations and meet customer requirements;

3. Organize the collection of product quality information, and promptly report the defects of the quality management system to the person in charge of the production enterprise, as well as product complaints, adverse event monitoring and product safety hazards;

1. Responsible for establishing and implementing the quality management system, and reporting the operation and improvement needs of the quality management system to the person in charge of the production enterprise;

2. Organize the internal medical device production quality management training in the production enterprise, and improve the employees' awareness and ability to comply with relevant laws and regulations and meet customer requirements;

3. Organize the collection of product quality information, and promptly report the defects of the quality management system to the person in charge of the production enterprise, as well as product complaints, adverse event monitoring and product safety hazards;

1. Responsible for establishing and implementing the quality management system, and reporting the operation and improvement needs of the quality management system to the person in charge of the production enterprise;

2. Organize the internal medical device production quality management training in the production enterprise, and improve the employees' awareness and ability to comply with relevant laws and regulations and meet customer requirements;

3. Organize the collection of product quality information, and promptly report the defects of the quality management system to the person in charge of the production enterprise, as well as product complaints, adverse event monitoring and product safety hazards;