EU Importer vs. Authorized Representative
Article 13 of the EU Medical Device Regulation (MDR) and the In Vitro Diagnostic Regulation (IVDR) includes a new requirement to appoint
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Article 13 of the EU Medical Device Regulation (MDR) and the In Vitro Diagnostic Regulation (IVDR) includes a new requirement to appoint
When you hear the word “importer” you might assume they are involved in the physical handling of your devices during the importation process. That’s logical...
Many medical device companies exporting to Europe have discovered that there is a new requirement to appoint an importer in the Medical Device Regulation
By now you certainly know that Article 13 of the EU Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) require you to appoint an importer for all...
No doubt you landed here because you did some research and figured out that you now need an EU-based importer. Perhaps you have been exporting medical
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