On 5 May 2017, the MDR and the IVDR were published in the OJEC. So the final countdown is now on until the two regulations come into force and a new era begins for medical device and IVD manufacturers.
We are glad to present to you the principal changes, new requirements for manufacturers and the schedule for the continued validity of existing certificates and the final opportunity to place products on the market on the basis of the old directives, and assist you in preparation for CE marking and MDR / IVDR compliance.
Find out more on 23 June 2017 in Düsseldorf at the business brunch ‘Medical Device Regulation – IVD Regulation’
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