Find out 5 major obstacles to patient centricity in clinical trials.

Run smoother, more successful regulatory affairs with accurate, complete, organized scientific and research information. Our regulatory solutions provide customers with outstanding support for product information and other regulatory documentation translation needs, while simultaneously meeting steep regulatory compliance requirements. 

Translate communications and mission-critical content for all your needs: marketing strategies, facilitating public and policy maker engagement, promoting corporate brands, attracting investors, disseminating information, and interacting with internal audiences. Rely on our focused, accurate communications adapted to your target audiences.

Prepare for the coming full implementation of MDR, more Notified Bodies, and increasing regulatory scrutiny and emphasis on clinical data quality. Whether you’re working on reclassified devices, companion diagnostics, or biotech products, we’ll help you adapt. Lionbridge’s robust and rigorous workflows for product labeling, IFUs, SSCPs, and other content will help you reach authorization in your target markets.

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