REGULATORY COMPLIANCE, SAFETY AND RISK
We understand your need for global documentation to support your medical device, regulatory and marketing activities quickly and cost effectively. The translation of information for use in conjunction with a medical device requires highly specialized insight into the many regulations that govern it. In addition to our exclusive focus on the life science industry, we have a team of highly specialized translation experts and linguists who are dedicated to managing the unique nuances of medical device projects including labeling, product manuals, patents and beyond. We know that patient safety, regulatory compliance, quality, scalability and price are your top priorities. As a result, we have dedicated an entire section of our Quality Management System to the translation of medical device content.
Our ISO 13485:2003 compliant translation processes, routine risk assessment procedures, technology solutions and intelligent use of translation memory ensure that you receive the highest quality translations available.