Life Sciences Translations

Translation and localization services specialized in EU Medical Device Regulation (MDR) compliance for medical device documentation, software, and marketing materials. Ensures regulatory-aligned translations across multiple languages while optimizing translation workflows through terminology databases and quality management.

Professional translation and localization services for medical documents, regulatory submissions, clinical trial materials, and healthcare publications across 140+ languages. Supports multilingual compliance, patient education materials, and global clinical communication with ISO 27001 certified data security and specialized medical terminology expertise.

The ISO 17100:2015 certification is an international standard designed to ensure the accuracy and reliability of medical device translations. It enforces strict qualification requirements for professional translators and reviewers, guaranteeing consistency and quality in medical device documentation through a structured translation and review process. This process helps minimize errors in product manuals, clinical reports, and regulatory documents, facilitating global market expansion. Furthermore, it fulfils the requirements of medical institutions and regulatory authorities that mandate international certification, enhancing your company’s credibility and boosting its competitive edge in the market.