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

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

Designed to guide you through IVDR requirements implementation to obtain and maintain CE mark for in vitro diagnostic medical devices. Learn more about IVD classification rules and conformity assessment routes. Increase your knowledge on General Safety and Performance Requirements in product development, performance evaluation and clinical evidence.

This course is designed to increase your understanding of IVDR key requirements to place your in vitro diagnostic device on the market.

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