post-market surveillance translation

Medical Device Post-Market Surveillance (PMS) Report Translation Use Case

Post-market surveillance (PMS) reports document ongoing device performance, safety, and risk management after medical device commercialization. Accurate translations ensure global regulatory compliance, consistent safety monitoring, and efficient communication of device performance internationally.

post-market surveillance translation

Case Study

Getting Ahead of the IVDR Tsunami

Download our white paper on protective strategies for navigating regulatory upheaval, translation demands and the evolving landscape of EU in vitro diagnostic compliance.