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Localization Lessons from EMA and FDA Submission Failures Global regulatory agencies such as the European Medicines Agency (EMA), U.S. Food and Drug Administration (FDA), Japan’s Pharmaceuticals and Medical Devices Agency (PMDA), and China’s National Medical Products Administration (NMPA) each maintain distinct language, formatting, and documentation requirements for life sciences submissions. While the industry continues to […]

AI and MTPE in Life Sciences Translation: What Works, What Doesn’t Advancements in artificial intelligence (AI) are transforming how life sciences organizations approach multilingual content. One of the most widely adopted applications is Machine Translation Post-Editing (MTPE), a process where AI-generated translations are reviewed and refined by professional linguists to achieve publication-quality results. In parallel, […]