Quality Systems

This presentation addresses the historical and contemporary link between Quality Systems and Regulatory requirements in the medical device and in-vitro diagnostic industry.

Other than the more traditional aspects of Quality Management System pertinent to the manufacturing environment, the presentation explores those QMS aspects between MD/IVD manufacturers and their suppliers of key products or services which will become more and more under the scrutiny of Notified Bodies.

Presented by: Maurizio SuppoMember of Board, EAAR; Principal Consultant, Qarad, Belgium