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Introduction Selecting a translation vendor for pharmaceutical or medtech work requires more than comparing prices. It is essential to evaluate capabilities that ensure regulatory compliance, terminological accuracy, data security and audit traceability. Below are...

Introduction Localizing documentation for medical devices requires technical accuracy, traceability and regulatory compliance. Translation alone is not enough. Instructions for use and labels must be adapted to local regulations, symbols, units and user practices. The...

Introduction Patient education videos must be clear, accessible and culturally sensitive. Voice-over and subtitles are complementary: audio supports comprehension, while captions reinforce the message for viewers who need visual aid. This guide presents concrete...

Introduction When a regulatory inspection arrives, the ability to present clear, auditable evidence of how translations were produced is critical. A well-structured audit package speeds the review, reduces questions, and protects the integrity of your regulatory...