EU Medical Device Regulation (MDR) 2017/745 – QMS Auditor

The Medical Device Regulation (MDR) is the legislation detailing the requirements that manufacturers must meet to place medical devices on the market in the European Union.

As more and more manufacturers now have their MDR Quality Management System (QMS) certificates, it’s imperative for continued compliance that they are able to perform audits against the requirements of the QMS MDR.

This course is designed to give you insights into how Notified Bodies may perform an MDR QMS compliance audit, using the topics of a typical MDR audit agenda as the basis. This will enable you to optimize your auditing skills and knowledge to boost your audit capabilities, gain confidence in planning and performing an effective EU MDR QMS audit, as well as ensuring continued compliance to the EU MDR (2017/245).

How will I benefit?

This course will help you to:

  • Perform audits against the EU MDR (2017/245) Quality Management System requirements
  • Ensure continued compliance against the EU MDR (2017/245) QMS requirements
  • Be confident that your organization can rely on competent EU MDR (2017/245) auditors

Please note: The training is in English.