Medical Translation

Medical translation is not a service you buy on price. It is a service you buy on expertise — because the distance between a correct medical translation and a dangerous one can be measured in a single misplaced modifier. Our medical translation division covers clinical trial documentation (protocols, informed consent forms, patient-reported outcomes, investigator brochures), regulatory submissions (EU MDR/IVDR compliance, EMA and national authority filings, CTD modules), patient information leaflets (PILs) and summaries of product characteristics (SmPCs), medical device documentation (IFU, labelling, risk assessments, technical files), pharmaceutical marketing and medical education materials, and healthcare provider communications (guidelines, training materials, CME content). Every medical translation is performed by a linguist with formal medical or pharmaceutical qualifications — physicians, pharmacists, biomedical scientists, or clinical research professionals who translate in their area of clinical expertise. We maintain compliance with ICH-GCP guidelines for clinical documentation and EU MDR requirements for medical device content. Quality assurance includes automated terminology verification, back-translation where required by regulatory authorities, and independent medical review. Timeline: 5-18 working days depending on regulatory complexity. Prices from €254.70.