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How the introduction of the new MDR & IVDR will impact you A big change in EU legislation is coming. The EU council and EU parliament are working on finalization of the new Medical Device Regulation (MDR) and In Vitro Diagnostic ...
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How the introduction of the new MDR & IVDR will impact you

How the introduction of the new MDR & IVDR will impact you

Time: on 25 October 2016, 16:30 - 17:30 (UTC + 01:00) Amsterdam, Berlin, Bern, Rome, Stockholm, Vienna

A big change in EU legislation is coming. The EU council and EU parliament are working on finalization of the new Medical Device Regulation (MDR) and In Vitro Diagnostic Directive Regulation (IVDR) that will replace some current Directives. These are the Medical Device Directive (93/42/EEC) and the EU’s Directive on active implantable medical devices (90/385/EEC) by the MDR. And in addition, the In Vitro Diagnostic Directive (98/79/EEC) will be replaced by the IVDR.

How can you prepare for these changes and how will this impact your organization? In this webinar we will inform you about the highlights of the new MDR and IVDR. Of course we will look into the necessary preparations to make the transition. You are more than welcome to ask your questions about this subject matter during and after the webinar. Our specialist team will be there for you.

Want to join? We look forward to welcoming you at our MDR/IVDR webinar. Please register on the right side of this invitation. Do you have colleagues or other people in your network who could benefit from the information shared during this webinar; DEKRA would be happy to welcome them.

Are you interested, but not available to join us live? Please register and receive a link to watch the webinar afterwards.

Tuesday

25

October 2016

This webinar has already occurred.