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Life sciences is our largest single domain. The translation work that comes through it is rarely simple. A medical device IFU has to satisfy regulatory reviewers in every market it ships to. A patient-reported outcome questionnaire has to mean the same thing in twelve languages. A clinical trial protocol cannot leave room for interpretation.
This section cover the questions our clients ask most often: what EU MDR and IVDR require linguistically, how to keep terminology consistent across long multilingual projects, what linguistic validation actually involves, and where AIcan be used in regulated content. Written from inside the work, not from outside it.