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Introduction Validating materials culturally with NGOs and communities ensures messages are understandable, respectful and effective. By using clear co-creation models, ethical incentives and measurable impact indicators, you increase acceptance, comprehension and...

Introduction Regulatory audits require clear evidence that translations are accurate, traceable and technically reviewed. Preparing the right documentation prevents findings, speeds up audit responses and protects regulatory submissions. Below you’ll find exactly what...

Introduction Localizing medical device documentation goes beyond translation: it requires adapting instructions, symbols and regulatory labeling to each market to ensure safety, compliance and usability. This guide provides a step-by-step checklist and technical...

Introduction A collaborative glossary is the backbone of terminological consistency in global projects. More than a word list, it’s a living system that reduces errors, speeds up workflows, and aligns translators, reviewers, clinical teams and product owners. This...