8th Medical Device Safety Monitoring & Reporting

Attending this 8th marcus evans event will allow attendees the opportunity to broaden and strengthen their safety measures while streamlining measures to maintain and meet regulatory sanctions. The Medical Device arena is constantly updating methods to best conduct device monitoring and reporting, it is imperative for companies to continually amend practices in order to maintain compliance, optimize device safety and maintain a competitive edge. With EU MDR compliance deadlines around the corner, this is a critical time for companies to identify and crowd check plans for meeting regulations. Additionally, in a world where technology is king, Medical Device manufacturers continue to find new ways to incorporate tech in the device realm, creating a more significant and diverse measure of safety than ever before.