On November 19th, Zhongjiu Flash Medical Technology Co., Ltd. conducted a special training on the "Administrative Measures for the Supervision and Administration of Medical Device Production" (Order No. 53 of the State Administration for Market Regulation). The purpose of this training was to thoroughly interpret the newly released administrative measures for the supervision and administration of medical device production by the State Administration for Market Regulation, ensuring the company's compliance in the field of medical device production and enhancing the level of quality management.

The training covered the five core chapters of the "Administrative Measures for the Supervision and Administration of Medical Device Production," including General Provisions, Production Licensing and Record Management, Production Quality Management, Supervision and Inspection, and Legal Liability.

The speaker was Zhu Kanghua from the Quality Department, who provided a detailed introduction to the purpose and scope of the administrative measures for the supervision and administration of medical device production. He emphasized the importance of regulating medical device production activities, strengthening supervision and administration, and ensuring the safety and effectiveness of medical devices. He also provided a detailed interpretation of the requirements for medical device classification management and production licensing and record filing, introduced the responsibilities of national and local drug regulatory departments in supervising and inspecting medical device production, clarified the legal liabilities for violations of the administrative measures for the supervision and administration of medical device production, and strengthened the legal and compliance awareness among employees.

After the training, He Xintan, the General Manager of Zhongjiu Flash, emphasized that company personnel must strictly comply with national laws and regulations and continuously improve the level of quality management. Through today's training, it is hoped that everyone can deeply understand and implement the "Administrative Measures for the Supervision and Administration of Medical Device Production," integrating the awareness of compliance into every aspect of daily work.

Through this training, employees have gained a more comprehensive understanding of the laws and regulations on the supervision and administration of medical device production, laying a solid foundation for the company's stable development in the field of medical devices. Zhongjiu Flash will further strengthen its awareness of regulations to ensure that medical device production activities are legal and compliant, contributing to public health and safety. In the future, the company will continue to pay attention to the latest developments in medical device regulatory policies and continuously enhance its core competitiveness.