Medical Devices
We perform Medical Device Translation ensuring Regulatory Compliance and Accurate Access
NN Translations is your trusted partner for precise and compliant translation solutions tailored to the medical device industry. With expertise in translating a wide range of medical devices and in-vitro diagnostics, we ensure compliance with stringent regulations, including EU regulations MDR 2017/745 and IVDR 2017/746.
Our skilled linguists, certified under ISO 9001 and ISO 17100, possess specialised knowledge of medical terminology and regulatory requirements.
From product manuals and clinical reports to regulatory documentation, we deliver accurate translations that facilitate market access and drive success in the highly regulated medical device sector. Trust NN Translations to bridge linguistic barriers and ensure your medical devices reach global markets with confidence and precision.
Why Us?
Specialised Expertise
Our team specialises in the medical device sector, offering translations that meet industry-specific terminologies and regulations
Regulatory Compliance
We adhere to the latest EU regulations, ensuring your documents are compliant and market-ready
Precision and Clarity:
Rigorous quality checks guarantee accuracy, supporting the safe use of medical devices across languages.
Global Reach:
Navigate international markets confidently, backed by translations that bridge linguistic and regulatory gaps.
Below is a list of common types of documents we translate:
- Product Manuals and User Guides
- Clinical Evaluation Reports (CERs)
- Technical Documentation
- Regulatory Submissions
- Summary of Safety and Clinical Performance (SSCP)
- Labeling and Packaging
- Patient Information Leaflets (PILs)
- Training Materials
- Post-Market Surveillance Reports
- Quality Management System (QMS) Documentation
- Sales and Marketing Materials
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