Quality Audits

audits 4


Medical Devices are marketed globally via country specific regulatory approval processes.  These processes involve strict adherence and compliance with regulatory requirements and quality management systems.  Audits are routinely used to confirm compliance and to provide feedback to manufactures on the success of their quality management systems.  In this course, participants will gain an understanding of the different types of audits performed on medical device manufacturers, key approaches to audits, the roles of auditors and auditees, and how to best prepare for audits conducted by regulatory agencies.



This course is available online, and can be taken at your own pace.

Please note: You must complete the course within 3 months of registration.

Course Features

  • Lectures 0
  • Hands-On Training 0
  • Duration 3 hours
  • Skill level All levels
  • Wet Lab No
  • Max Students 75
  • Assessments Yes