Join us for our new clinical masterclass series of webinars. The timelines for ensuring your product maintains EU market access under the new, more stringent Medical Device Regulations (MDR) are challenging.
These five insightful webinars will help you focus on various aspects of the MDR, from looking at post-market clinical follow-up, to helping you with your medical device software and when a clinical evaluation is required. In addition, participants will gain a better overall understanding of the post-market requirements as listed under Articles 86 and 87 of the MDR.
Please see individual webinar information and dates below.