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Life Sciences and MDR Consultancy

Is all your product documentation and labeling content compliant with new regulations? Our experts are ready to do a full assessment and let you know if there are any gaps to fill.

With new regulatory requirements just around the corner, it’s important to make sure your entire organization is compliant with the requirements set out in the EU MDR. In some areas you may need additional support, and for that we recommend our MDR consulting services.

How can we help?

  • Content translatability assessment – a review of your content through the eyes of a translator, providing direction to your content creators and technical writers on clarity and terminology that has not yet been codified or defined.
  • MDR readiness – an evaluation to benchmark translation readiness for MDR
  • MDR terminology database – access to a terminology database created specifically for the MDR regulations
  • Linguistic asset review – an assessment of your current localization style guides, glossaries, and translation memory strategies
  • Content strategy review – an assessment of your current content strategy to implement MDR and use “lessons learned” for the next wave of EU or global regulations