The EU MDR & IVDR regulations have been published and the timeline is set for manufacturers that want to continue to sell their devices in Europe. The EU MDR & IVDR Conference (hosted by the producers of the annual UDI Conference) will bring together leading European experts to provide critical information and guidance to help you prepare to meet the timelines.
More importantly, you will be exposed to a philosophical and strategic approach to efficiently managing your devices from a global vantage point, rather than just an immediate compliance effort. It is our intention to raise the critical awareness that medical device manufacturers need to learn to manage devices to stay in regulatory and commercial compliance in the ever-expanding global UDI-related regulatory and commercial framework.
Features of the Conference will include:
Medical Device Manufacturers who want to continue to sell devices in Europe that are facing the MDR & IVDR regulations should attend. We also encourage those involved with regulations, quality, compliance, IT, business development, engineering, and other disciplines to attend. Group Discounts are offered. Details are on the registration page.