Ensure patient safety with medical device certification

In the highly regulated world of medical device manufacturing, organisations have a duty to ensure patient safety and to show that every device meets both customer expectations and applicable regulations.

In this whitepaper, we hear from one of LRQA’s technical experts about the common findings identified during ISO 13485 audits and how by taking extra consideration of these key areas including management, internal audit and advisory notices, organisations will find that their auditing process runs more smoothly.