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Medical Devices – Post Authorization Translation Services
Experienced, reliable post-authorization translation assistance for MDR compliance.
Create and share easily understood, accurate content and patient communications in any language. Trust Lionbridge’s team to support you through the MDR’s increased emphasis on post-market surveillance and handle your medical device translation requirements. We bring years of experience with PSUs and SUSARs, product and safety updates, and post-market clinical activities. Learn more.
Lionbridge’s Thought Leadership for Medical Devices Post-Authorization Translation Services
We understand the complexities and regulatory challenges of life sciences medical device translations. More from our experts:
