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Accurate, Compliant IB Translations for Global Trials

Ensure your Investigator’s Brochure is translated with the precision required for global regulatory submissions. Sesen delivers medically accurate, submission-ready translations backed by native linguists with life sciences expertise and in-language MD or PhD reviewers. Our ISO 17100 and ISO 9001:2015 certified workflows align with ICH-GCP and regional regulatory expectations, supporting ethics committee approvals, investigator training, and successful trial activation across all major markets.

What Sets Our Investigator’s Brochure Translations Apart

Global translation coverage across all major trial regions, including Asian, European, and Latin American languages.

Expert validation of scientific content to ensure clinical accuracy and regulatory clarity in each target language.

Structured, audit-ready translation processes designed for quality, traceability, and continuous improvement.

Translations tailored to the expectations of authorities such as EMA, FDA, PMDA, ANVISA, and Health Canada.

Professionally formatted, submission-ready deliverables with optional regional review and reconciliation support.

Ready to Learn More?

Discover how Sesen delivers accurate, regulatory-ready Investigator’s Brochure translations to support global clinical trials. Explore our full service offering and see why leading sponsors and CROs trust us for multilingual clinical content.

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