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Learn how AI Document Analysis helps you break down complex documents into clear summaries, structure, and key insights in minutes.

Create consistent content faster with AI style guide generator. Learn how to build, update, and use style guides that work for both teams an

An AI glossary generator turns your existing documents into structured, consistent glossaries in minutes. Here's how it works and when to us

Post-market surveillance Translation under EU MDR carries continuous translation obligations. Learn what documents need translating.

AI translation in eLearning can cut costs and speed up delivery, but used without oversight, it hurts learner outcomes.

Medical device label requirements under EU MDR explained. Learn what needs translation, what symbols cover, & how labels work in practice.

Not all translation QA tools catch the same errors. Compare Xbench QA, Verifika QA, and CavyaQA to pick the right fit for your quality stand

Milestone Localization, ISO 13485, 17100 & 9001 certified, translation and localization agency announced the launch of its new website

The EU MDR regulation is evolving in 2025. Understand the real impact on translation requirements, digital content, and compliance strategy.

Understand EUDAMED translation requirements under MDR/IVDR. See what documents need translation, & how to plan for May 2026 compliance.

EU-QRD Compliance guide for pharma teams. Learn EMA translation needs for SmPC, PIL, & labeling to avoid Day 180 linguistic review failures.

Learn why Document Analysis matters in translation projects. Identify complexity, plan workflows, and deliver smoother, more accurate result