We help Life Sciences organisations achieve better regulatory and business outcomes through accurate, compliant, and scalable multilingual content, supported by consultancy in compliance, regulatory affairs, legal, and marketing – along with a trusted local network of distributors. We support around 180 languages, working with medical device manufacturers, pharmaceutical sponsors, CROs, and eCOA providers.

We translate, validate, and optimise:
• IFUs
• SSCPs
• DoCs
• Labels & packaging
• SPCs, PILs & EMA content
• COAs and patient-facing materials

⭐ What Sets Us Apart – Compliance + Business Outcomes

We’re not just a language service provider. We are a strategic partner focused on content excellence, regulatory precision, and measurable business outcomes.

Our work is:

• MDR/IVDR-compliant
• EMA-aligned and terminologically consistent
• Conceptually equivalent and culturally adapted
• Audit-ready, submission-ready, and globally scalable
• Strengthened by our network of consultants in regulatory affairs, compliance, legal, marketing, and local distribution – enabling greater business outcomes under one roof

⭐ How We Improve MedTech Business Outcomes

• Ensure multilingual compliance with MDR/IVDR and national requirements
• Produce accurate translations for EU and global launches
• Support regulatory submissions with precise, language-aligned documentation
• Deliver audit-ready content that eliminates rework
• Provide full traceability for notified body reviews
• Optimise workflows to save time, reduce cost, and prevent delays
• Combine linguistic expertise with regulatory, compliance, legal, marketing, and distribution support

NN Translations

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