The Medical Devices Regulation (MDR) is the legislation detailing the requirements that manufacturers must meet to place medical devices on the market in the European Union.
Learn some key requirements about Annex VII of the MDR and gain a better understanding of why notified bodies may be seen to behave differently and in a much more detailed way than what organisations may have previously experienced.
How will I benefit?
This course will help you:
- Appreciate the requirements of Annex VII from the MDR
- Gain a better understanding of some key Notified Body requirements within the MDR
Who should attend?
Quality, Regulatory, Technical professionals working in the Medical Device industry
What will I learn?
By the end of the course, you will be able to:
- Establish the requirements detailed in Annex VII of the MDR
- Appreciate the Notified Body prospective and approach when assessing against the MDR
- Gain an overview of the clinical evaluation requirements
- Understand audit duration and approach of Notified bodies as per the MDR
What's included?
- This is an online, interactive on-demand course.
- The course content is both detailed and engaging, with explanations, activities, and knowledge checks to enhance your learning.
- Duration 1 hour
On completion, you’ll be awarded an internationally recognized BSI Training Academy certificate
