iso 13485 audit checklist (2)

What are the ISO 13485 Audit Requirements

In simple terms, an ISO 13485 audit is a review of your business to determine whether it complies with contemporary standards for medical device quality management. A quality management system (QMS) i...
13 September 2023 ·
0
· 1 · john

Understanding the role of ISO 13485 Documents in QMS

For medical device manufacturers, ensuring the safety and efficacy of their products is an absolute priority. This is where a robust Quality Management System (QMS) comes into play. The ISO 13485 stan...
06 July ·
0
· 3 · Miana Charles