As part of new requirements relating to the forthcoming EU / UK Medical Device Regulation, the ASR Division Equipment and Technology Group are implementing a Quality Management System (QMS) compliant with ISO 13485. 

The purpose of this course is to provide training to those within the ETG around how the QMS functions, and the various roles and expectations of multi-disciplinary professionals within this. 

The QMS utilises an electronic web-based system called iPassport for managing many activities, so a number of topics will relate directly to iPassport.