Featured Resources

Discover our most popular and recently published white papers and e-books—expert-developed resources designed to support translation, localization, and regulatory success across the life sciences industry. These select titles offer actionable insights for clinical trial teams, regulatory affairs professionals, medical device manufacturers, and global marketing leaders.

The Future of Translation in Clinical Trials

Type: White Paper

Abstract: Explore emerging trends in multilingual content for decentralized clinical trials (DCTs), including eConsent, eCOA, and patient-facing materials—key to global regulatory compliance and trial success.

Multilingual Labeling Strategies for Global Drug Products

Type: E-Book

Abstract: A comprehensive guide to managing multilingual labeling, packaging, and artwork translation for pharmaceuticals—covering EMA and FDA requirements, QRD templates, and version control workflows.

AI in Life Sciences Translation: Use Cases, Risks & Governance

Type: White Paper

Abstract: Understand how AI and MTPE are transforming translation workflows in pharma and medtech, with insights on quality assurance, human oversight, and regulatory considerations.

Software Localization for Clinical & Medical Applications

Type: E-Book

Abstract: Practical best practices for localizing clinical platforms, patient portals, and digital health tools—addressing linguistic validation, UI/UX adaptation, and compliance across global markets.

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Unlock our complete collection of white papers and e-books on life sciences translation, localization, regulatory compliance, and AI innovation. These expert-developed resources are designed to help pharma, biotech, medical device, and healthcare organizations succeed globally.

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