Our Expert Approach to Life Sciences Translation
We combine our network of specialist linguists with advanced AI technology and ISO-certified processes. This ensures your complex scientific content is always translated with technical precision, regulatory compliance, and cultural nuance for global success.
Navigating Your Challenges
We appreciate the nuance of this sector. Our medical translation services help you overcome the challenges of maintaining scientific accuracy and consistent terminology, ensuring you meet strict compliance standards and accelerate your global time-to-market.
- Navigate global regulations
- Patent applications
- Pharmacovigilance
- Informed consent forms
- Medical device IFUs
- Clinical trial protocols
FAQs
We guarantee accuracy through our ISO-certified quality management systems (ISO 9001, 17100, and 27001). Our rigorous process involves multi-stage reviews by subject matter experts and is enhanced by AI-powered tools that check for terminology consistency, ensuring the highest level of precision for your critical documents.
Our global network consists of over 8,000 linguists who are not only native speakers but are also qualified subject matter experts. Many have direct industry experience in areas like clinical research, biotechnology, and pharmaceuticals, ensuring they understand the complex terminology and context.
Absolutely. Our services are specifically designed to meet strict international regulatory standards, including the EU’s Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR). Our translations always meet the highest compliance requirements for global market access.
We use an advanced “human-in-the-loop” model. Our secure machine translation processes provide a high-quality initial translation. This output is improved by our Agentic AI models, which are then used again to leverage against MQM scoring. It is then meticulously reviewed, edited, and perfected by our human subject matter experts to ensure absolute accuracy, nuance, and compliance.
We work across a range of specialist areas, from clinical trial management and patient engagement to medical devices and pharmacovigilance. Example documents that we can translate include: IFUs, PILs, ICSR’s, DSUR, CIOMS, PSUR’s, Line Listings for Regulatory authorities, Medical Records, SUSAR, Periodic line listings, Aggregate Reports, Articles/Publications, Toxicology reports, Drug registration documents, and more.
Get in touch to find out exactly how we can help you.
