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.

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

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

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

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