Medical Translation
Clinical documentation, patient materials, pharmaceutical submissions, and medical device instructions translated to regulatory standard.
About this service
Medical translation errors have consequences. A wrong dosage unit. A misidentified contraindication. A patient information leaflet that understates a side effect. These are not academic failures; they are regulatory and sometimes clinical failures. We translate medical content with translators who have specific backgrounds in medicine, pharmacology, clinical research or medical device engineering. No medical content is handled by a general language translator. Our coverage includes clinical trial documentation including consent forms, investigator brochures and protocol summaries; patient information leaflets and package inserts; regulatory submission documents for EMA, AEMPS and equivalent bodies; medical device user manuals and IFU documents; diagnostic report templates; medical journal manuscripts; and continuing medical education materials. For clinical trial documents, we include compliance annotations indicating where translation choices follow specific EMA or ICH terminology guidance. All files are delivered with a translator declaration where required by the receiving institution.
What is included
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