Navigate evolving regulatory standards for medical devices, starting with your R&D processes. Rely on our experience to meet MDR standards by integrating safety and surveillance data with documentation from the design stage. Trust us with your:

IQ/OQ/PQ documentation

Clinical validation

Clinical performance

Risk management

Be prepared for the final phase of MDR implementation and ensure your pipeline will benefit from the extended deadlines. More Notified Bodies are coming on stream, but backlogs are mounting. We understand the clock is ticking for legacy certifications. Lionbridge will support you through strategic choices about reclassified devices, companion diagnostics, and biotech products. Our robust and rigorous workflows help customers reach authorization in all their target markets. We assist with: 

Product labeling 

IFUs, 

SSCPs 

other content. 

Benefit from ready-made solutions for med-tech companies entering software and consumer electronics markets. We have the scale, facilities, and diverse industry portfolio to service traditional content types. Trust us with your shared services, marketing, corporate communications, eLearning, and more. For high volumes and more diverse content, consider our state-of-the-art Smaⁱrt MT™ and Smaⁱrt Content™ solutions.