Learn about the key requirements, concepts, and the overall process for CE marking under the Medical Devices Regulation (MDR).

This on-demand course is designed to increase your understanding of MDR key requirements to place your device on the market.

This course will guide you through MDR implementation. Find out best practices to implement a compliant QMS and prepare a thorough Technical Documentation package to obtain CE mark for your medical device.

This course is designed to give you insights into how Notified Bodies may perform a 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).

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 (2017/745).

Increase your understanding of medical device software lifecycle processes, classification rules and development activities to meet regulatory requirements.

This one-day intensive course increases your understanding on key requirements for technical documentation for medical devices, in accordance with MDR.

Bring world-class quality standards to your business with our introduction to ISO 9001 quality management training course. 

Look for a more flexible way to learn? This course is also available on-demand