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Medical Device Translation Services


Medical Device Translation Services Overview

Medical Device submissions across the world are dependent on accurate translation of technical information, although regarded last by many. A simple mistake in translation can delay or bring the approval process to a standstill, thereby causing the applicant loss of time and resources, impacting the overall costs for companies. More and more companies are opting for Medical device translation services to make this process more efficient.

With technical writing expertise and proficiency in 100+ global languages, Freyr provides medical device translation services with a team of experienced medical language translators and editors who can assist you creating error-free translations abiding to context of the targeted regional language. A Quality Management System (QMS) with full compliance to ISO 17100:2015 and ISO 9001:2008 standards is a testament to the technical expertise at Freyr. Freyr’s Medical Device Translation Services includes both General Translation and Scientific Translation Services.

Freyr Expertise and Advantages

Freyr Expertise

  • Instructions for Use / IFU Translation
  • Medical Device operation, maintenance and installation manuals, instruction and user guides
  • Manufacturing Process Descriptions
  • Product catalogues
  • Clinical training materials
  • Package inserts and labels
  • Brochures and web content
  • Regulatory compliance documents
  • Informed consent forms for clinical trials
  • Validated back translation and sworn translations in certain countries
  • Localization of Medical Device software, translation of resource files
  • Software application interfaces and documentation
  • Patents for medical and surgical devices
  • General and Scientific Translation
  • Translation of Agency guidelines published in local

Freyr Advantages

  • Dedicated local affiliates in multiple countries across the world
  • Cost-effective and timely delivery
  • Expert translators and language specialists to simplify complex technical jargon
  • Qualified team of experts with hands-on experience across all categories of Medical Devices
  • Customized approach based on the complexity, class and type of the product involved
  • Services tailored to meet region-specific Regulatory complexities
  • Strong relationship with local agencies of the countries
  • Structured approach to ensure quick market access