E-learning content is available on demand
Course Details
Overview
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.
