Recently, an audit team from Boston Life Sciences, a global leader in the life sciences field, visited Shenzhen Pray- Med Technology Co., Ltd. (hereinafter referred to as "Pray- Med") to conduct a two-day special factory audit for suppliers. Focusing on core dimensions such as quality management system, production compliance control, and data integrity, this audit aims to comprehensively assess Pray- Med's supply chain guarantee capability and compliance level, laying a solid foundation for deepening strategic cooperation between the two parties. The general manager of Pray- med and the person in charge of core departments including production, quality, and R&D accompanied the audit throughout the process.
At the kick-off meeting of the audit, the general manager of Pray- med extended a warm welcome to the audit team of Boston Life Sciences, and elaborated on the company's development history, core business layout, technological R&D capabilities, and global compliance strategy. He stated that Pray- med has always regarded "quality compliance as the root and technological innovation as the soul" as its development philosophy, strictly abiding by international medical industry standards such as ISO 13485, and establishing a full-process quality management system covering R&D, production, inspection, and warehousing. This audit is not only a test of the company's comprehensive strength, but also an important opportunity for the two parties to jointly explore the global high-end medical market.
Subsequently, in accordance with industry norms and cooperation agreement requirements, the audit team of Boston Life Sciences carried out systematic on-site inspections and document reviews. In the production workshop, the audit team went deep into the Class clean production area, carefully inspected the production process, equipment operation status, clean environment control and other conditions of core products, In the quality control laboratory, the team conducted a comprehensive inspection on the calibration of testing instruments, traceability of experimental data, sample management processes, etc., focusing on data integrity and record standardization to ensure that each test result is traceable and verifiable.
During the document review phase, the audit team conducted a detailed review around core materials such as quality management system documents, production operation guidelines, employee training records, and Corrective and Preventive Action (CAPA) management system, and in-depth evaluated the implementation effects of Pray- med in compliance management, risk control and other aspects. The two parties conducted in-depth discussions on topics such as the update dynamics of medical industry regulations, supply chain risk management and control, and continuous quality improvement. The audit team put forward targeted optimization suggestions based on global industry practices, and the relevant person in charge of Pray-med responded one by one and clarified the follow-up improvement direction.
After one days of comprehensive audit, the audit team of Boston Life Sciences highly recognized Pray-med's compliance management level, production control capability and technical strength. The person in charge of the audit team said: "Pray-med has demonstrated a rigorous attitude and solid foundation in quality management system construction, production process control and data integrity assurance, which fully meets the high standards required by the life sciences field for suppliers. The results of this audit are satisfactory, providing strong support for the two parties to further expand the boundaries of cooperation and achieve mutual benefit and win-win results."
The quality director of Pray-med stated that the company will take this audit as an opportunity to earnestly implement the optimization suggestions put forward by the audit team, continuously iterate the quality management system, strengthen full-process compliance control, and continuously improve product quality and supply chain stability. In the future, the two parties will take compliant cooperation as the cornerstone, deepen collaboration in high-end medical product R&D and global market expansion, and jointly provide safer and more efficient medical solutions for global patients.
The successful conduct of this factory audit by Boston Life Sciences not only confirms Pray-med's comprehensive competitiveness in the medical supply chain field, but also demonstrates the company's confidence and strength in exploring the global high-end market. As an innovative enterprise in the medical technology field, Pray-med will always adhere to the bottom line of compliance, drive development with technological innovation, and work hand in hand with global high-quality partners to build a high-quality new ecology of medical supply chain.
Recently, an audit team from Boston Life Sciences, a global leader in the life sciences field, visited Shenzhen Pray- Med Technology Co., Ltd. (hereinafter referred to as "Pray- Med") to conduct a two-day special factory audit for suppliers. Focusing on core dimensions such as quality management system, production compliance control, and data integrity, this audit aims to comprehensively assess Pray- Med's supply chain guarantee capability and compliance level, laying a solid foundation for deepening strategic cooperation between the two parties. The general manager of Pray- med and the person in charge of core departments including production, quality, and R&D accompanied the audit throughout the process.
At the kick-off meeting of the audit, the general manager of Pray- med extended a warm welcome to the audit team of Boston Life Sciences, and elaborated on the company's development history, core business layout, technological R&D capabilities, and global compliance strategy. He stated that Pray- med has always regarded "quality compliance as the root and technological innovation as the soul" as its development philosophy, strictly abiding by international medical industry standards such as ISO 13485, and establishing a full-process quality management system covering R&D, production, inspection, and warehousing. This audit is not only a test of the company's comprehensive strength, but also an important opportunity for the two parties to jointly explore the global high-end medical market.
Subsequently, in accordance with industry norms and cooperation agreement requirements, the audit team of Boston Life Sciences carried out systematic on-site inspections and document reviews. In the production workshop, the audit team went deep into the Class clean production area, carefully inspected the production process, equipment operation status, clean environment control and other conditions of core products, In the quality control laboratory, the team conducted a comprehensive inspection on the calibration of testing instruments, traceability of experimental data, sample management processes, etc., focusing on data integrity and record standardization to ensure that each test result is traceable and verifiable.
During the document review phase, the audit team conducted a detailed review around core materials such as quality management system documents, production operation guidelines, employee training records, and Corrective and Preventive Action (CAPA) management system, and in-depth evaluated the implementation effects of Pray- med in compliance management, risk control and other aspects. The two parties conducted in-depth discussions on topics such as the update dynamics of medical industry regulations, supply chain risk management and control, and continuous quality improvement. The audit team put forward targeted optimization suggestions based on global industry practices, and the relevant person in charge of Pray-med responded one by one and clarified the follow-up improvement direction.
After one days of comprehensive audit, the audit team of Boston Life Sciences highly recognized Pray-med's compliance management level, production control capability and technical strength. The person in charge of the audit team said: "Pray-med has demonstrated a rigorous attitude and solid foundation in quality management system construction, production process control and data integrity assurance, which fully meets the high standards required by the life sciences field for suppliers. The results of this audit are satisfactory, providing strong support for the two parties to further expand the boundaries of cooperation and achieve mutual benefit and win-win results."
The quality director of Pray-med stated that the company will take this audit as an opportunity to earnestly implement the optimization suggestions put forward by the audit team, continuously iterate the quality management system, strengthen full-process compliance control, and continuously improve product quality and supply chain stability. In the future, the two parties will take compliant cooperation as the cornerstone, deepen collaboration in high-end medical product R&D and global market expansion, and jointly provide safer and more efficient medical solutions for global patients.
The successful conduct of this factory audit by Boston Life Sciences not only confirms Pray-med's comprehensive competitiveness in the medical supply chain field, but also demonstrates the company's confidence and strength in exploring the global high-end market. As an innovative enterprise in the medical technology field, Pray-med will always adhere to the bottom line of compliance, drive development with technological innovation, and work hand in hand with global high-quality partners to build a high-quality new ecology of medical supply chain.
