adverse event

Adverse Event Translation Use Case

Pharmaceutical and medical device companies rely on accurate translations of adverse event (AE) source documents to meet regulatory requirements, ensure patient safety, and facilitate global reporting. Fast, precise, and compliant translations help streamline pharmacovigilance processes and prevent delays in drug and device approvals.

adverse event

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.