With the definite text published less than a week ago, we welcomed over 150 industry representatives interested in the new Medical Devices Regulation. Erik Vollebregt kicked off the seminar with his presentation about Transitional regime, bottlenecks and major MDR items impacting transition.  Sippie Formsma of the Dutch Healthcare Inspectorate followed with her presentation about Implementation of the MDR in the Netherlands. Last but not least Gert Bos of QServe talked about How to prepare and execute an MDR transition plan.