ESG Report 2024

37 During the Year, Zhuhai Company successfully passed a five-day online GMP inspection by COFEPRIS, an official organisation in Mexico, which is the eighth time that the Company has successfully passed the GMP certification by COFEPRIS. The inspection focused on the production and quality management of the sterile APIs Ceftriaxone Sodium and Cefotaxime Sodium. The inspectors conducted a comprehensive audit of the company's utilities, production and inspection sites, and quality system documentation system through online video. In the concluding meeting, the inspector gave high praise to the company's production site and quality system management, and fully affirmed Zhuhai Company's excellent performance in quality management. In the future, Zhuhai Company will continue to adhere to the international advanced standards, continuously improve the quality of products to meet the needs of global customers, and contribute to the cause of human health. Zhuhai Company successfully passed the eighth online GMP inspection by the Mexican COFEPRIS Professional quality management personnel are an important part of the Group's quality assurance of pharmaceuticals. To enhance the professional capabilities of quality management personnel, the Group conducts various training sessions regularly. These sessions help them gain a deeper understanding of the operational mechanisms and critical aspects of various procedures, further strengthening the professionalism and integrity of quality control. The training’s scope covers latest edition of Chinese Pharmacopoeia, production process, quality, as well as mastering inspection and verification methods and grasping product release procedures. The training sessions mainly involves centralised lectures, with assessments conducted through oral or written tests to ensure that quality management personnel fully grasp the necessary knowledge, thereby maintaining a high standard of quality management within the Group. In addition, the Group has set up a section, namely “Quality in The United Laboratories”, on our corporate website. The section includes legal knowledge, the Group's quality requirements, training information and a forum to provide all our employees with an online knowledge base and a platform for learning and communication on quality, and to optimise the channels and effectiveness of quality training. 7.1.3 Quality Management Training To enhance employees' quality management capabilities and awareness, the Group has organised a series of quality training sessions aimed at strengthening employees' understanding and application of quality standards. For example, the Zhuhai Company conducted a total of 10,070 internal training sessions this year, including 8,053 planned training sessions and 2,017 unplanned sessions, along with 26 external training sessions. These training programs primarily cover regulatory knowledge, job competencies, operational skills, and management abilities, thereby comprehensively improving employees' professional quality and practical work capabilities. Quality Management Training The Group has formulated and implemented relevant management systems for label packaging materials in accordance with laws and regulations. All package inserts and labels comply with the requirements in the “Provisions on the Administration of Pharmaceutical Directions and Labels” and are subject to examination, filing and approval by the National Medical Products Administration. 7.1.4 Product Labelling and Description Environmental, Social and Governance Report 2024 The United Laboratories International Holdings Limited