The seven-dimensional station activity of the "Medical Device Production Quality Management Specification and Supervision Capacity Improvement Training Class" of the Jilin Provincial Drug Supervision and Administration Bureau was successfully held.
Release time:
2024-10-10 11:08
Source:
On the morning of September 24, 2024, the Jilin Provincial Drug Supervision and Administration Bureau held an offline training session on "Medical Device Production Quality Management Specifications and Regulatory Capacity Enhancement" at Jilin Qiwei Biotechnology Co., Ltd. Director Zhang Jiaxiu led a team of over 30 experts from the training program to visit Qiwei Bio.
This event included two agendas: exchange and sharing, and on-site visits. At the beginning of the event, Director Zhang Jiaxiu gave an opening speech, clarifying the purpose of the event. Yang Liyong, General Manager of Qiwei Bio, extended a warm welcome to the experts from the training program, expressed sincere gratitude for the trust of the Provincial Bureau, and introduced the company's development history, main business, and future development goals.
At the meeting, Qiwei Bio shared and exchanged information on three aspects: "Supplier Audit and Management", "Production Process Management of Gel Dressing Products", and "Finished Product Release Management of Class II Medical Device Dressings".
During the event, the expert group gave full affirmation and high praise to Qiwei Bio's quality management system, including its hardware and software facilities, R&D capabilities, supplier evaluation and audit, production process management, and quality management. They also expressed their expectations for the future of Qiwei Bio, encouraging the company to leverage its strengths, cultivate specialized fields, strengthen R&D innovation, actively expand the market, continuously improve scale efficiency, and become a benchmark enterprise in the Class II medical device industry in Jilin Province.
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