Medical device translation services
Instructions for use that meet EU-MDR in every market you ship to.
IFUs, labelling, clinical documentation and marketing materials, translated by linguists with genuine medical-specialization knowledge, with EU-MDR compliance and consistency across every document treated as the baseline, not an upsell.
An IFU error is not a typo. It is a market-access problem.
EU-MDR requires device information in the official language of every member state you sell into. That makes translation a compliance dependency, not a courtesy.
EU-MDR compliance as the baseline
Every IFU and label is treated against the language requirements of the market it ships to, not translated once and assumed to travel.
Translators with genuine medical specialization
Not general linguists working from a glossary: translators with real background across medical specializations, who understand what an IFU is actually instructing someone to do.
QA enforcement, not QA intention
Automated checks for terminology, numbers and formatting run after every translation step. Patient-safety language does not reach delivery unchecked.
Reuse across your full document set
IFUs, labels, catalogues and marketing materials draw on the same memory, so approved terminology stays identical across every document type, every time.
The memory is exportable, on request, any time
Built from your device terminology, it stays your asset, in portable format, with glossaries and term bases included.
Efficient enough to make new markets viable
Cost-effective processes without compromising quality, so expanding into an untapped market is a translation decision you can actually make.
Life sciences and medical device documents we translate.
From the IFU in the box to the technical file your notified body reviews, our specialist linguists translate every document that supports your device across its lifecycle.
Data sheets
Declarations of conformity
Development safety update reports (DSURs)
Directions for use (DFUs)
Installation manuals
Instructions for use (IFUs)
Manufacturing procedures
Marketing materials: catalogues, specialist press articles, presentations, websites and multimedia
Medical device recall notifications
Packaging content
Product labels
Quick reference guides
Regulatory compliance documents
Technical files and SOPs
Training, operating and maintenance manuals
User guides
IFUs and labels that look right in every language.
Translated text grows, shrinks and changes direction, while labels and IFUs have fixed space, symbols and regulatory layouts. Our DTP team works in your original files so every language version is ready for print or digital release, without rebuilding the layout.
Explore multilingual DTP →InDesign, FrameMaker and Illustrator files
Labels, packaging artwork and leaflets with limited space
Symbols, tables and diagram callouts kept intact
Print-ready PDFs and eIFU outputs
TUBE keeps regulated content moving at the pace your filings need.
Machine translation controlled by your approved glossary and translation memory, and a memory you own, for device manufacturers where IFU updates and market expansion are constant.

This is built for device manufacturers regulated under EU-MDR.
You place devices in multiple EU member states with distinct language requirements
IFUs and labelling are revised with every product or regulatory update
Marketing and catalogue content need to reach untapped markets alongside regulatory documentation
Consistency of terminology across documents matters for both compliance and patient safety
What we translate for medical device companies
Instructions for use and user manuals
Labels and packaging
Clinical and regulatory documentation
Marketing materials and product catalogues
Translations for medical device manufacturers.
Download our free report to see how we help life sciences and medical device companies meet EU-MDR language requirements and get every market version right.
The EU-MDR language requirements explained
Why multilingual device content needs specialist translators
How certified processes keep your translations accurate

See what EU-MDR-ready translation looks like for your device line.
Send us a recent IFU and your current memory. We will report the real reuse rate, the compliance gaps we find, and what your next market launch would look like.












