International laws and regulations stipulate that key documentation relating to medical devices must be translated in order to be sold in different territories across the globe. Our ISO certified processes, coupled with expert translators and Account Managers with subject matter expertise, you can be sure that your material will be translated by a company that has a sound understanding of the medical device industry. We have experience of translating all types of documentation relating to Class I through to Class III devices, using specialist medical glossaries and guidelines, and in line with applicable directives. Our expertise covers the following document types:
- Operation and Maintenance Manuals
- Regulatory Compliance
- Packaging Inserts/Labels
- Manufacturing Process Descriptions
- Marketing Material
- Informed Consent Forms
If you would like to discuss your translation project with one of our specialist medical Account Managers, please contact us for more information today.