Certified Translation of Instructions for Use for Medical Devices
The primary objective of the translation is to provide users with clear and understandable guidelines for properly using medical devices. The most important aspect to
Translation and localization services for medical equipment manufacturers operating in the global market.
It refers to any equipment, apparatus, instrument, implement, machine, appliance, implant, prosthesis, reagent for in vitro use or software intended to be used, alone or in combination, for human beings, for one or more specific medical purposes.
The greater the risk factor and invasiveness, the more crucial it is that the translation is correct. There is no room for error.
Whether you’re marketing your products overseas or you’ve got production sites in a foreign country, translation plays a vital role in your product’s life cycle.
We’re certified to ISO 17-100:2015 and our team of life science experts is carefully handpicked to guarantee precision and consistency in your multilingual content.
+60 language
pairs
+20 language
solutions
ISO 17100:2015 certified translation process
Tipo de traducciones para productos sanitarios
Garantizamos la calidad exigida por las normativas europeas a los fabricantes y distribuidores de productos sanitarios y biotecnología, empresas farmacéuticas y dermocosméticas, así como en el ámbito de los ensayos clínicos y registros.
Ayudamos a las empresas de productos sanitarios y otros sectores de ciencias de la vida a conquistar nuevos mercados trasladando sus principales mensajes al idioma de su nuevo público objetivo.
We’ve been supporting medical equipment manufacturers for over 15 years, always keeping up-to-date on the latest innovations and regulations related to the medical device sector in Europe and the rest of the world.
Here’s a quick over of our latest medical device translation projects:
Certified Translation of Instructions for Use for Medical Devices
The primary objective of the translation is to provide users with clear and understandable guidelines for properly using medical devices. The most important aspect to
Certified Translation of Instructions for Use for Medical Devices
The primary objective of the translation is to provide users with clear and understandable guidelines for properly using medical devices. The most important aspect to
New European Union Medical Device Regulation
What is MDR? The MDR is the new regulation for medical devices and sanitary products. Its main objective is to establish new requirements for the
New European Union Medical Device Regulation
What is MDR? The MDR is the new regulation for medical devices and sanitary products. Its main objective is to establish new requirements for the
Translation
Interpreting
Localization
Other services
Localization
Other services
MDR is the new set of regulations governing the production and distribution of medical products in Europe. In this article, we tell you all about this new regulation.
