By taking into account the local environment in which a medical device will be used, by whom, and how best to communicate with them. Your customer satisfaction can be maximized and total cost of support can be minimized. Our technical medical translators are experts in your field and your device’s operating environment, and are backed by our ISO 17100 certified processes.
Our technical medical translators are expert in your field.
Operating, Maintenance and Installation Manuals
Development Safety Update Reports (DSURs)
Instructions for Use
Regulatory Compliance Documents for European Union and Asian countries
Software Application Interfaces and Documentation
Package Inserts and Labels
Patents for Medical and Surgical Devices
Manufacturing Process Descriptions
Expand Your Markets While Addressing Risk
Cross-border localization projects are critical to reaching new markets and achieving product success. Regulatory compliance, cultural understanding, language difference, and even linguistic nuance all figure prominently in how well a device can move from one market to its expanded markets. We address your needs through our ISO 17100 certified processes.