Medical devices

How to build a localisation workflow that complies with Article 50 of the EU AI Act 

How to build a localisation workflow that complies w...

How to build a localisation workflow that complies w...

8 October 2026

Lucy Vauclair

Discover the texts and translations that fall under Article 50 in your industry and unlock a robust localisation...

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Article 50 of the EU AI Act has come into force: do your texts meet the new transparency obligations? 

Article 50 of the EU AI Act has come into force: do ...

Article 50 of the EU AI Act has come into force: do ...

8 September 2026

Lucy Vauclair

At a glance:     Introduction Do your texts need an AI label? Since 2 August 2026, some migh...

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EU MDR translation requirements: What medical device manufacturers need to know in 2026

EU MDR translation requirements: What medical device...

EU MDR translation requirements: What medical device...

2 February 2026

The Sandberg team

EU MDR translation requirements determine which medical device documents must be translated, into which language...

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Exporting medical devices

Exporting medical devices

Exporting medical devices

1 September 2021

William Hagerup

No longer part of the European Union, the regulatory burden of exporting can be substantial for a UK company tha...

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