Presentations MDR Implementation Seminar

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.


Navigate through our knowledgebase

Related articles

Article

Netherlands to adopt medical devices anti-corruption legislation

As we say in Dutch: the day that you knew that would come is finally here. The legislative proposal to grant the Healthcare Inspectorate (IGZ) IGZ enforcement powers in the field of…

Read more

Article

Final MDR and IVDR texts published

As Agent Smith said: “You hear that Mr. Anderson?… That is the sound of inevitability…”. Today’s EU Official Journal contains the final final final texts of the MDR (finally numbered as Regulation (EU)…

Read more

Article

MDR and IVDR to be published this Friday

Mark 5 May 2017 in your calendar – this date will be a landmark for EU medical devices law because the MDR and IVDR will be published in the EU Official Journal….

Read more