This one-day intensive course helps medical device manufacturers understand the benefits and impact of ISO 14971:2019. It’s ideal for anyone in a quality assurance, regulatory, engineering or manufacturing role. We also recommend a basic knowledge of medical device development, quality assurance and ISO 13485:2016.  

Through a mix of practical activities, classroom learning and group discussion, you will learn risk management terminology and the stages of the risk management process. You’ll also be able to identify links between ISO 149721:2019, ISO 13485:2016, MDR 2017/745 and IVDR 2017/746. 

Available as in-person training or on-demand eLearning, this ISO 14971:2019 requirements training course is designed to improve risk management efforts across your organization. 

How will I benefit?

  • Understand, interpret and explain key requirements of ISO 14971:2019
  • In-depth knowledge of how ISO 14971:2019 links to ISO 13485 and the regulations; MDR 2017/745 and IVDR 2017/746
  • Carry out risk management for medical devices within your organization
  • Gain an internationally recognized BSI training certificate from your partner in learning