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Multilingualism is the key to the success of your medical devices abroad. Our aim as your transaction service provider: to maximise this success using language as a medium. We provide perfect service every day, in addition to our technical expertise. For texts that ensure compliance and safe use in line with the MDR, in any language.
Request medical device translation
Instructions for use (IFUs) / technical data sheets / product brochures / technical documentation / operating instructions / SOPs / websites / manuals / marketing authorisation documents / training material / catalogues / user apps / and much, much more…
Numerous regulations, such as the MDR, ISO 9001 and ISO 13485, ensure that medical devices and their supporting documents meet all safety-related requirements. Our translators are experts in the relevant terminology and all current regulations.
Regardless of whether your text is intended for lay persons, service technicians or healthcare professionals: our experienced specialists translate your documents competently into the required local language, precisely tailored to your users. For maximum safety – and maximum success of your products on the world market.
In addition to specialist medical technology translations, we offer further services to save you time and help you reduce time-to-market for your medical devices.
Foreign languages are typeset directly in your file format to create the final layout, whether InDesign or other formats. Our layout designers adapt the translated texts to the required length for your packaging texts and other documents, so the translation is in the right place from the start.
Take advantage of our foreign language layout services to avoid errors and save time.
Manufacturers of suture material, prostheses, orthoses and compression garments, wound care and glycaemic control products, surgical technology such as mechanical respirators, cannulas and catheters and other medical devices trust the high-quality technical medical translations provided by Transline.
Our service portfolio for medical technology device texts and labelling offers you tailor-made solutions in all aspects of language management. From clinical research and registration through to the launch of your medical devices, your personal contact at Transline will support you every step of the way.
Top quality translation for user safety you can trust.
As a member of the Transline Group, we offer not only in-depth knowledge and exceptional process expertise – Transline is also ISO 13485 certified for medical devices. The standard applies to the entire lifecycle and supply chain of the device, including the product’s supporting documentation and its translation. For the benefit and safety of your patients and users.
