To strengthen professional expertise in medical device quality management and internal auditing, the Center invited professional instructors from BSI to deliver a series of practical courses on quality management systems and simulated audits of GMP facilities. The courses were designed to help students and industry partners gain an in-depth understanding of audit procedures and key implementation considerations, while cultivating internal auditors equipped with both professional knowledge and practical skills.

Date: August 26–27, 2026
Time: 9:00 a.m.–5:00 p.m.
Venue: Room 625, Sixth Academic Building, National Taipei University of Technology
Organizer: High-Value Biomedical Materials Research and Commercialization Center, National Taipei University of Technology

The latest ISO 13485 quality management system applies throughout the medical device supply chain and covers the entire product life cycle.

Through this training course, participants gained a solid understanding of the relevant requirements and key auditing principles while further enhancing their practical capabilities in medical device quality management and regulatory compliance.