Our company recently held a 13485 system training. The purpose of this training is to enhance our company's quality management capabilities in the field of medical devices, further improve product quality and customer satisfaction, and strengthen our competitiveness in the manufacturing industry of medical equipment.

As a company with a good reputation in the field of medical device electronics manufacturing, we have been committed to continuous improvement and innovation to ensure that our products comply with industry standards and regulatory requirements. In this training, we invited professional lecturers from the field to help participants gain a deeper understanding of the core elements and implementation methods of the 13485 system through various forms such as professional knowledge, case studies, and interactive discussions.

The 13485 system refers to the international standard for the quality management system of medical devices. Compared to the quality management system ISO 9001, it focuses more on the unique needs and regulatory requirements of the medical device industry. Based on this system, we will further improve our quality management system to ensure that the entire process of product design, procurement, production, and after-sales service meets high-quality standards. This training not only enhanced the participants' understanding of the 13485 system, but also improved the practical abilities of our employees in quality control, product validation, and continuous improvement. We believe that through such training, our team will become more professional in quality management, risk management, and compliance, providing customers with more reliable and safer products.

I hope that colleagues who participate in the training can apply the knowledge they have learned to their daily work and make positive contributions to the development of the company and the improvement of customer satisfaction.