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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.
This course will help you to:
Upon completion of this training, you will be able to:
This course is ideal for you if you’re in a QA, Regulatory, Engineering or Manufacturing role involved in medical device design, development and manufacturing.
This training course is HRD Corp claimable programme.
On completion, you will be awarded an internationally recognized BSI Training Academy certificate.
Reach out and see how we can help guide you on your path to sustainable operational success.