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The Medical Device Regulation (MDR) is a comprehensive set of European Union (EU) rules that govern the production, sale, and distribution of medical devices. These devices play a crucial role in diagnosing, monitoring, preventing, and treating medical conditions, ensuring they meet the highest standards of safety and performance. This short course will focus on how the MDR prioritizes safety, effectiveness, and the highest standards of public health within the EU.
On-demand - training that’s even more flexible
BSI’s on-demand courses are market-leading and available 24/7. Developed by top subject matter experts, they contain the same high-quality content you will find in our tutor-led training, but with the added benefit of being able to learn at your own pace and at any time.
This course will help you:
Upon completion of this course, you will be able to:
All staff in medical device organizations.
This is an online, interactive on-demand course.
Courses are available 24/7 and you can learn at any time and from any place that suits you – you just need an internet connection.
You can learn as fast or as slowly as you want to. You can also take breaks at any time in the course and pick up where you left off when you are ready to continue
During the access period, you can go back and repeat parts or all the course
to refresh and reinforce what you have learned
The course content is both detailed and engaging, with explanations, activities, and knowledge checks to enhance your learning.
Reach out and see how we can help guide you on your path to sustainable operational success.