ISO 13485:2016 Requirements

Discover ISO 13485 quality management and how it can improve your medical devices business.

Our Understanding ISO 13485 Medical Devices course provides an overview of quality management system requirements.

Find out how the standard impacts the design, development and production of medical devices – improving quality and efficiency. And learn why ISO 13485 compliance is essential to meeting customer and legal requirements.

Take the first steps towards your own medical devices quality management system, drawing links with other quality standards including ISO 14971 medical device risk management.

This Online Course is available in English.

Please note: the price stated is excluding local taxes.


You will need knowledge and experience of medical device manufacturing