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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
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:
