From a single clinical document to a multilingual package for a product launch or regulatory submission - we help you communicate medical and technical information accurately across languages.
Handled by translators with relevant professional backgrounds, with approved terminology preserved across every document and language.
Biotechnology research documentation · veterinary product documentation & summaries · animal health regulatory submissions · laboratory protocols & technical manuals.
Over more than 27 years, medical device manufacturers, pharmaceutical companies, diagnostics firms, biotech organizations and healthcare providers have trusted us with their most sensitive documentation.
Pharmaceutical product information and healthcare materials for one of the world's largest pharma companies.
Diagnostics systems and medical software documentation for a leading IVD manufacturer.
Digital pathology and imaging system documentation.
Consumer & professional medical device documentation.
Pharmaceutical docs incl. Japanese-language specialist texts.
Pharmacopoeia and pharmaceutical quality texts.
Conference interpreting for haematology events across Europe.
Simultaneous interpreting for European medical congresses.
Veterinary biologicals documentation.
Multilingual patient-facing and clinical content.
Multilingual interpreting for healthcare industry meetings.
Regulatory and compliance documentation.
Cardiology software localization across nine European languages.
Clinical trial and pharmaceutical documentation.
Medical translation requires deep familiarity with medical terminology, regulatory frameworks and the documentation standards that govern the sector across jurisdictions.
We are familiar with the documentation requirements of the European Medicines Agency (EMA) and the frameworks governing medical devices and pharmaceuticals in the EU.
Yes. We regularly translate technical documentation, instructions for use, labelling and related materials for medical device manufacturers operating under EU MDR and IVDR frameworks.
Yes. We have worked with both multinational pharmaceutical manufacturers and regional pharma companies on regulatory, clinical and product documentation.
Yes. We translate clinical protocols, informed consent forms, case report forms, ethics committee submissions and related materials.
Yes. We provide certified translations of medical records, discharge summaries, diagnostic reports and other clinical documents for official and administrative use.
Yes. Many medical translation projects can be completed on accelerated schedules. Contact us to discuss your timeline and we will advise on the options available.
Yes. All documents are handled under strict confidentiality procedures and GDPR requirements. We are happy to sign non-disclosure agreements where required.