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The EU Medical Device Regulation – what is new for importers and distributors?
Related topics:
MedTech, Commercial
Overview
- Definition of economic operators in the MDR.
- Impact of new regulatory requirements on importers and distributors.
- Working with legal manufacturers.
- Next steps.
Speaker
Matthias Bürger
Vice President QA/RC EMEA
Zimmer Biomet, Switzerland
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This is the presenters’ personal opinion and does not necessarily represent true facts, the official views or policy of their organisation, nor the views of Evidence Life Science.