We have successfully completed the April recertification audit of our Medical Devices Quality Management System.
The new ISO 13485 Certificate ensures operational continuity through 2029. It enables Assel to execute long-term manufacturing strategies in collaboration with international medical market leaders, while also opening doors to new, innovative projects in the field of medical technology.
Later this year, we plan to implement an additional quality management system. Our goal is not only to strengthen our current competencies but, above all, to increase our readiness for the dynamically changing needs of our clients and increasingly stringent legal regulations.
We invite you to read the full article on Evertiq.
