SumaLatam Anniversary News 2014

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...

Introduction Quality and regulatory compliance are non-negotiable in medical translation. Knowing relevant standards and certifications helps you evaluate vendors, reduce risk and ensure traceability. This article outlines the most useful standards, what to request...