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.