{"id":1070,"date":"2026-01-13T11:02:48","date_gmt":"2026-01-13T11:02:48","guid":{"rendered":"https:\/\/www.omnilingua.co.uk\/healthcare\/?page_id=1070"},"modified":"2026-01-13T15:54:13","modified_gmt":"2026-01-13T15:54:13","slug":"mdr-translation-compliance-checklist","status":"publish","type":"page","link":"https:\/\/www.omnilingua.co.uk\/healthcare\/mdr-translation-compliance-checklist\/","title":{"rendered":"MDR Translation Compliance Checklist"},"content":{"rendered":"

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Planning Your MDR Translation Compliance<\/strong><\/h1>\n

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The EU Medical Device Regulation (MDR) requires manufacturers to provide documentation in the official language of each member state where their device is sold. For many companies, this means translating technical documentation, Instructions for Use (IFUs)<\/a>, labelling, and marketing materials into multiple European languages \u2013 all while maintaining consistency and regulatory compliance.<\/p>\n

Our free MDR translation compliance checklist helps you plan and track this process across a 12-month timeline. Based on our 25 years of experience supporting medical device manufacturers with MDR translation requirements<\/a>, we’ve broken the journey into four manageable phases: Assessment, Preparation, Implementation, and Finalisation.<\/p>\n

Use the interactive checklist below to:<\/p>\n