Notified Body designation and scope, the impact of Brexit and Competent Authority and Notified Body interpretation of the regulations. Make sure you are up to date!

MedTech TV: EU MDR and IVDR implementation challenges

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At MedTech Summit in Brussels (June 2019) we interviewed three industry insiders on the hottest topics facing the industry for MedTech TV. Watch the full interviews here.


EU MDR: 5 challenges facing organizations - Oliver Christ, NSF International

Oliver Christ, Health Sciences Managing Director EMEA, NSF International, discusses the biggest impacts and challenges that the European Medical Device Regulations will have on organizations and how PROSYSTEM is supporting preparations.



Implementing the EU MDR and IVDR with Oxford Global Resources

Nicolas Perez, Account Manager at Oxford Global Resources, shares his advice to medtech organisations approaching the EU's new regulations for medical devices and in-vitro diagnostic medical devices.



Technologies to facilitate the EU MDR - Marc Miller TransPerfect

Marc Miller, Division President at TransPerfect Medical Device Solutions, discusses the technologies that facilitate translation of the EU MDR, as well as the challenges industry is facing with EU MDR and IVDR implementation.


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