MDR and IVDR EU Conference
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12/5/2017 to 12/6/2017
When: Tuesday, December 5, 2017

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Features of the Conference will include:

-The impact of MDR & IVDR compliance and adoption for  medical device manufacturers
-Dissection of the technical components of the regulations (re-certification, reclassification, UDI) and resources to provide ongoing support
-The importance of value beyond compliance – creating an overarching approach
-The matrix concept of managing devices in the rapidly expanding global regulatory landscape
-MDR & IVDR related standards development and ongoing harmonization efforts
-The similarities and differences between the EU and US UDI Regulations
-Discussion of the new processes and players that must be internalized
-Defining Notified Bodies and the European Commission responsibilities and impacts


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