Course Details

Medical Device Regulation: Lessons Learnt

Course Area

Medical Devices


Available for 90 days after enrollment

Course Fee

No charge

E-learning content is available on demand!


Course Details


The Medical Device Regulation (MDR) Date of Application (DoA) is approaching. The timelines for ensuring your product maintains EU market access under the new, more stringent MDR are challenging. BSI Notified Body wants to share some of our experience working on Technical Documentation submitted under the MDR.

Key takeaways and learning objectives

This webinar will offer notified body insights for all people involved in working towards an MDR application, whether you are a novice or have significant experience of working with a notified body. We will not focus on any specific medical device type, more on the gaps we see in current applications.

Presenter information

Join BSI's Kevin Madden, Team Training Lead and Technical Team Manager in the Orthopaedic and Dental technical team, to hear the critical lessons we have learnt and how you can use these to improve your submissions to BSI. We will share notified body experience and common pitfalls and learnings. Kevin will be joined for the Q&A section by Chris Wylie, Global Head, Orthopaedic & Dental Devices, BSI.

Live Online Classes

Certified, convenient, and interactive, with no travel costs.

Private Class

Interested in a private or customized version of this course? Request a quote.


For questions regarding any of our courses, contact us or call 1.800.862.6752.


For questions regarding any of our courses, contact us or call 800.217.1390 (USA) 800.862.6752 (Canada)

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