On the one hand, the online training course of medical devices is mainly to improve enterprises' understanding and implementation of relevant standards and promote the more standardized and efficient development of the medical device industry. On the other hand, it is also to guide the drug regulatory authorities at all levels to continuously carry out the normal supervision of medical devices, urge the production enterprises to fully implement the main responsibility of quality and safety, strengthen the pertinence and effectiveness of supervision and inspection, improve the inspection ability and level, enhance the understanding and implementation of relevant regulations and standards, and promote the more standardized and efficient development of the medical device industry.