Regulatory requirements are tightening. Language markets are expanding. And medical device manufacturers face more pressure than ever to communicate clearly — across dozens of languages, without error.

At Geo, we’re built for this.

We combine multi-layered quality assurance with translation memory and terminology management to keep your content consistent, accurate, and audit-ready. For high-volume device programmes, this doesn’t just improve efficiency — it protects your product.

Our translators know the devices they work on. From robotic surgery systems to everyday inhalers, we handle user manuals, clinician instructions, and patient-facing eLearning — keeping usability and human factors front and centre throughout.

We use AI-assisted translation carefully and strategically — accelerating turnaround times, handling large content volumes, and reducing costs without cutting corners.

Then our human subject-matter experts take over. Specialists in medical device translation, they refine terminology, verify regulatory alignment, and ensure every final document meets the standards your product depends on.

20 years of experience. 12,000 linguists. 330+ language pairs.

We bring deep medical device expertise to every project. We design custom workflows around your product, your team, and your timeline — and where it adds real value, we bring subject-matter experts such as surgeons or engineers directly into your translation cycle.

We work to full ISO compliance across every engagement:

ISO 17100 – Translation services
ISO 9001 – Quality management systems
ISO 13485 – Medical devices
ISO 18587 – Machine translation post-editing