Localisation by Experts in the Industry

We support Pharma, BioTech and MedTech teams with localisation from start to finish, adapting your regulatory and technical, patient-facing and safety reports and adverse events documentation materials with precision to meet the linguistic and cultural requirements of the UK.

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Our team of experts have 10+ years of experience working with…

Regulatory and Technical Copy

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Patient-Facing Copy

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Safety Reports and Adverse Event Documentation 

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For every project we guarantee:

A Dedicated Project Manager

Your project manager will guide you through the process, keep you updated and ensure your project is delivered on time.

Written to UK Regulations

Your content is translated to meet MHRA requirements, so that patient information, device instructions and regulatory submissions are accurate, compliant and ready for the UK market.

100% Accuracy

Every document in a project goes through careful translation, expert review and final checks to ensure its accuracy and consistency throughout the entire project.

Experts in Life Sciences

Our translators have medical, scientific and technical backgrounds, so they understand your content and terminology.

Fully Secured Projects

Documents and data are fully secure and handled in line with UK regulations, giving you complete peace of mind.

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