Partner with Lionbridge’s life sciences translation services team for solutions designed specifically for your devices, markets, and patients. Our dedicated medical device teams develop workflows customized for your products’ life cycles, from R&D to approval and beyond. We utilize a deep network of specialized linguists, and the world’s leading device makers trust our project teams. With a quality system certified since 2008 for ISO 13485 compliance, we ensure quality outcomes you can always depend on.Get more news about medical device translation services,you can vist our website!

Faster Speed to Market
Never experience delays or challenges meeting deadlines with our “in-time-every-time” delivery. Enter your target medical device markets faster.
Reliable Regulatory Compliance
Stop worrying about regulatory compliance with Lionbridge’s proven track record of translating product information, labeling, manuals, and user instructions. We’re ISO 13485-certified and experienced with EU MDR regulations for labeling, user instructions, clinical trials, and UDI systems.
Improved Drug/Product Safety
Trust our decades-long track record of translating content for medical device users. We’re experienced with medical terminology and plain language for device labeling, product information, user instructions, and manuals.
Clinical Trial Expertise
Depend on our team’s deep expertise in clinical investigations, clinical trials, and experience translating related content for MedTech manufacturers.
Reduced Costs
Rely on our cutting-edge technology (including AI), workflows, glossaries, and high-quality translations all significantly slash translation costs.