Smoothly Navigate MDR Implementation and Reach Authorization

Medical Devices – Regulatory Translation Services

Ensure MDR compliance and optimize your pipeline.

More Notified Bodies are coming on stream, but backlogs are mounting. Lionbridge understands the tight timelines for legacy certifications. We’ll help you with your medical device translation needs, including:

Preparing for the final phase of MDR implementation.
Ensuring your pipeline benefits from extended deadlines
Making strategic choices about reclassified devices, companion diagnostics, and biotech products.
Reaching authorization in all target markets
Handling product labeling
Translating IFUs, SSCPs, and other content

Multilingual Content Centralization for Smooth MDR Implementation

Medical device manufacturers are in a time crunch to meet new EU requirements for multilingual documentation. Here’s what to consider when picking an LSP for assistance.

Lionbridge’s Thought Leadership for Medical Devices Regulatory Translation Services

We understand the complexities and regulatory challenges of life sciences medical device translations. More from our experts: 

The Extended Medical Devices Regulation Transition

Learn why the EU Medical Devices Regulation transition was extended, as well as how this impacts medical device manufacturers and service partners.

The Unique Language Challenges of IVDs and the EU IVDR

The EU IVDR brings a myriad of language requirements similar to those for MDR. Get expert guidance from Lionbridge’s life sciences translation services team in our whitepaper.

Language Requirements Under the EU MDR

Medical device manufacturers and distributors have a limited window to comply with various EU MDR changes. Read the Lionbridge whitepaper on language requirements to learn how regulation will impact your company.

Get in Touch

Send a message about how we can assist with your medical device translation services needs.

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