ISO 14971:2019 Risk Management for Medical Devices: Requirements Training Course

Level Understanding Duration 1 day

Available to book: Public classroom View dates and book now

This course is designed to provide you with an understanding of ISO 14971:2019 and the impact it has on the design, development, manufacturing and lifecycle of medical devices. It will also provide medical device manufacturers with knowledge of how ISO 14971:2019 links with the ISO 13485:2016 standard and the MDR 2017/745. Practical activities throughout the day will give you the opportunity to apply your skills, implementing risk management activities so that these can be embedded within the organization on completion of the course.

How will i benefit?

This course will help you to:

Identify the key requirements of ISO 14971:2019
Interpret and communicate the key requirements and expectations of ISO 14971:2019 to your organization
Gain knowledge of how ISO 14971:2019 links to ISO 13485 and the regulations; MDR 2017/745 and IVDR 2017/746
Apply the fundamental risk management activities for medical devices within your organization

Upon completion of this training, you will be able to:
- Define risk management terminology
- Explain how risk management relates to the product lifecycle
- Outline the stages of the risk management process
- Define the key deliverables of the risk management process
- Apply risk management principles within your organization
- Identify the links between ISO 14971:2019, ISO 13485:2016, MDR 2017/745 and the IVDR 2017/746
This course is ideal for you if you’re in a QA/Regulatory/Engineering/Manufacturing role involved in medical device design, development and manufacturing.
- Delegate workbook
- On completion, you'll be awarded an internationally recognized BSI Training Academy certificate

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