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Stay ahead in a highly regulated, global industry with thought leadership from Sesen. Our blog covers trends, challenges, and innovations in pharmaceutical, biotech, and medical device translation. Whether you’re managing global clinical trials or launching multilingual patient support platforms, our insights help you make informed decisions.
Expert Commentary on Life Sciences Translation Challenges and Innovations
Explore our most timely and high-impact articles curated to support pharmaceutical, biotech, medical device, and CRO professionals navigating multilingual compliance and global market entry. These insights reflect Sesen’s deep expertise in regulatory translation, clinical localization, and AI-enhanced workflows for life sciences.
What’s shaping the future of life sciences localization? From regulatory harmonization to AI-driven content reuse, discover the trends redefining translation workflows across the healthcare and biopharma sectors.
Learn how life sciences organizations overcome regional terminology discrepancies, evolving submission formats, and multilingual compliance requirements for EMA, FDA, PMDA, and NMPA.
A practical look at hybrid translation, post-editing of machine translation, and where human linguistic expertise remains critical for risk-sensitive content.
Factors to evaluate when selecting a translation partner for ICFs, eCOA, site agreements, and patient-facing materials, from linguistic validation to in-country reviews.
Real-world examples of avoidable mistakes in regulatory translations. Explore how translation gaps have delayed product approvals and how to prevent similar risks.
Explore Key Themes in Life Sciences Translation and Localization
Dive into high-impact topics that matter most to global pharmaceutical, biotech, medical device, and healthcare organizations. From regulatory strategy to AI integration, Sesen’s articles offer actionable insights to support multilingual compliance, patient engagement, and market expansion.
Translation strategies for global submissions and multilingual documentation aligned with evolving regulatory standards.
Best practices for ensuring language accuracy and compliance in multinational studies.
Technical and regulatory translation considerations across the product lifecycle.
Tailored translation strategies for drug development and scientific communications.
Ensuring accessibility and engagement in multilingual health tech and education.
Smart tools and frameworks that enhance translation accuracy, speed, and consistency.
Localization as a core component of international expansion and brand growth.
Insights from Senior Linguists, Regulatory Advisors, and AI Technologists
Tap into expert knowledge from the professionals behind Sesen’s high-precision language solutions. These recurring columns provide in-depth commentary on the technical, regulatory, and technological aspects of life sciences translation. Each piece is authored by Sesen’s senior team members who work at the intersection of language, compliance, and innovation.
A biweekly Q&A column featuring insights from Sesen’s certified medical translators. Topics include terminology harmonization, source text ambiguity, regulatory language pitfalls, and techniques for ensuring clinical accuracy across languages.
Detailed case-based articles exploring real-world localization projects. Go inside our workflows for multilingual clinical trial materials, regulatory submissions for emerging markets, and global medical device launches. Learn how complex challenges are solved with precision and strategy.
Conversations and insights from Sesen’s AI and localization engineering teams. Topics include neural MT optimization, SesenGPT model updates, translation memory scaling, Veeva and CMS integrations, and how automation is safely applied in regulated environments.
Real-World Results in Life Sciences Translation and Localization
See how Sesen delivers measurable outcomes for leading pharmaceutical, biotech, and clinical research organizations. These featured success stories demonstrate our ability to manage complex multilingual projects with precision, speed, and regulatory rigor.
Sesen supported a major pharmaceutical client with end-to-end translation of CTD modules, SmPCs, PILs, and labeling content for simultaneous EMA, FDA, and PMDA submissions. The project covered 28 languages, integrated terminology QA, and met all local regulatory requirements within compressed timelines.
A global CRO partnered with Sesen to improve enrollment outcomes by localizing ICFs, patient brochures, site training documents, and ePRO interfaces for use in diverse geographies. The effort improved recruitment timelines and ensured linguistic compliance across languages.
For a fast-scaling biotech company, Sesen implemented a customized translation memory strategy that significantly reduced repetition costs while improving linguistic consistency. The solution supported the localization of scientific literature, regulatory content, and promotional materials across 10+ languages.
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Access additional expert content to support your global life sciences initiatives. These resources complement our blog insights with in-depth guidance, terminology tools, and live industry discussions.
From regulatory submissions to clinical trial materials and global product launches, Sesen combines linguistic accuracy with subject matter expertise. The insights shared in our blog reflect the same quality we bring to every client engagement.