Focus on Quality Compliance, Consolidate Development Foundation ——Our Company Holds Special Training on the New Version of Good Manufacturing Practice for Medical Devices
Release time:
2026-05-25
To fully implement the training requir
ements specified in Announcement No.107 of 2025 issued by the National M
edical Products Administration concerning the new version of Good Manufacturing Practice for Medical Devices, further strengthen the construction of the company’s quality management system, and enhance all staff’s awareness of compliance and quality control capabilities, our company organized a special training session on the new regulations on May 22, 2026, with all employees in attendance.
Centering on the core revisions of the new GMP for medical devices, this training highlighted the essence of regulatory updates, supervision trends and key implementation points. It mainly elaborated on specific requirements and implementation approaches for quality management system upgrading, as well as challenges and countermeasures brought by regulatory changes to production and business operations. During the session, the company’s Management Representative analyzed key clauses and practical difficulties in combination with industry cases and actual business conditions, enabling all employees to accurately grasp core requirements and integrate regulatory principles into daily work.
The training helped all participants fully comprehend the connotation of the new standards and clarify new objectives and requirements for quality management, laying a solid foundation for the full implementation of the revised norms, system optimization, and improvement of corporate compliance management and quality assurance capacity. Going forward, the company will take this training as an opportunity to continuously carry out regular quality training, ensure the effective operation of the quality management system, standardize production and operational activities strictly, fully guarantee the quality and safety of medical devices, and boost the high-quality development of the enterprise.
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E-mail:aachek@aachek.com
Phone:+8613558238093
ADD : 13 Lushan Road, Lushan Industrial Park, Xicheng Economic Development Zone, Guilin, 541199 Guangxi PR. China
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