MDR – the single biggest change to medical device regulations in Europe since CE marking was introduced in 1993 – is less than 18 months from taking effect.

If you haven’t begun planning your transition, now is the time to act. It is imperative that medical device manufacturers and other economic operators be proactive and adopt a highly strategic and programmatic approach to conformance.

Brian Moan’s LIVE WEBINAR will provide medical device quality professionals, quality directors, managers, engineers and auditors with a summary of the program, clarify the timeline, discuss key areas that he’s found to be sticking points for manufacturers, answer any questions attendees might have, and outline the services that Maetrics can provide to support MDR implementation and management.

         1:00PM GMT         

For questions regarding the MDR webinar, please email infoeurope@maetrics.com or reach us by phone on +44 115 921 6200