technical document translation

Medical Device Technical File Translation Use Case

Medical device technical files include essential regulatory, clinical, manufacturing, and design documentation required for global market approval. Accurate translation ensures regulatory compliance, streamlines market entry, and supports device safety, performance, and quality standards worldwide.

technical document translation

Case Study

Getting Ahead of the IVDR Tsunami

Download our white paper on protective strategies for navigating regulatory upheaval, translation demands and the evolving landscape of EU in vitro diagnostic compliance.