L10N Solutions provides precise, regulatory-compliant translation and localization services for global clinical research programs. Our specialized linguists support pharmaceutical companies, CROs, biotech firms, and medical device manufacturers throughout the entire clinical trial lifecycle — from protocol development to post-marketing safety updates.
Every translation is handled by domain expert linguists trained in ICH-GCP, EMA, FDA, and international regulatory frameworks. This ensures linguistic accuracy, scientific clarity, and compliance for all documents required in multi-country clinical trials.
Translation of protocols, IBs, consent forms, regulatory submissions, safety reports, and more — ensuring global trial readiness.
Expert localization of ePRO/eCOA screens, patient diaries, questionnaires, and educational materials for improved comprehension.
End-to-end language support for global study sites, investigators, regulatory teams, and monitoring teams across all study phases.
Full linguistic validation workflow for PROs including forward translation, reconciliation, back translation, and cognitive debriefing.