The new MDR is finally in force after several delays during the last year, but what changes from the MDD to the MDR and what does this mean for Medical Class I products, products meant for OR, ICU – patient vicinity?

The presentation is about an overview of the regulations especially regarding the Class I devices and the transition to the new regulations, what it takes to introduce a product with the new regulation, what does one have to consider? steps and guidelines. And finally are there deviations on national level beyond the regulations?

Sounds like a dry topic? – it is actually, I will try to make it as juicy as possible in my presentation.
Ray van Someren, AdLink (namens Arcobel)

Meld u aan voor een gratis beursbezoek.

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